ClinVar

NM_001276345.2(TNNT2):c.*37C>T

Gene:

TNNT2:troponin T2, cardiac type [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q32.1

Genomic location:

• Chr1: 201359173 (on Assembly GRCh38)
• Chr1: 201328301 (on Assembly GRCh37)

Preferred name:

NM_001276345.2(TNNT2):c.*37C>T

HGVS:

• NC_000001.11:g.201359173G>A
• NG_007556.1:g.23505C>T
• NM_000364.4:c.*37C>T
• NM_001001430.3:c.*37C>T
• NM_001001431.3:c.*37C>T
• NM_001001432.3:c.*37C>T
• NM_001276345.2:c.*37C>TMANE SELECT
• NM_001276346.2:c.*37C>T
• NM_001276347.2:c.*37C>T
• LRG_431t1:c.*37C>T
• LRG_431:g.23505C>T
• NC_000001.10:g.201328301G>A
• NM_001001430.2:c.*37C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs149240770

NCBI 1000 Genomes Browser:

rs149240770

Molecular consequence:

• NM_000364.4:c.*37C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001001430.3:c.*37C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001001431.3:c.*37C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001001432.3:c.*37C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001276345.2:c.*37C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001276346.2:c.*37C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001276347.2:c.*37C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]

Observations:

5