ClinVar

NM_001276345.2(TNNT2):c.*66G>A

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

1q32.1

Genomic location:

• Chr1: 201359144 (on Assembly GRCh38)
• Chr1: 201328272 (on Assembly GRCh37)

Preferred name:

NM_001276345.2(TNNT2):c.*66G>A

HGVS:

• NC_000001.11:g.201359144C>T
• NG_007556.1:g.23534G>A
• NM_000364.4:c.*66G>A
• NM_001001430.3:c.*66G>A
• NM_001001431.3:c.*66G>A
• NM_001001432.3:c.*66G>A
• NM_001276345.2:c.*66G>AMANE SELECT
• NM_001276346.2:c.*66G>A
• NM_001276347.2:c.*66G>A
• LRG_431t1:c.*66G>A
• LRG_431:g.23534G>A
• NC_000001.10:g.201328272C>T
• NM_001001430.2:c.*66G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs3729998

NCBI 1000 Genomes Browser:

rs3729998

Molecular consequence:

• NM_000364.4:c.*66G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001001430.3:c.*66G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001001431.3:c.*66G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001001432.3:c.*66G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001276345.2:c.*66G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001276346.2:c.*66G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001276347.2:c.*66G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]