ClinVar

NM_000208.4(INSR):c.1124-81G>T

Gene:

INSR:insulin receptor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

• Chr19: 7172515 (on Assembly GRCh38)
• Chr19: 7172526 (on Assembly GRCh37)

Preferred name:

NM_000208.4(INSR):c.1124-81G>T

HGVS:

• NC_000019.10:g.7172515C>A
• NG_008852.2:g.126486G>T
• NM_000208.4:c.1124-81G>TMANE SELECT
• NM_001079817.3:c.1124-81G>T
• NC_000019.9:g.7172526C>A

This HGVS expression did not pass validation

Links:

dbSNP: rs41412545

NCBI 1000 Genomes Browser:

rs41412545

Molecular consequence:

• NM_000208.4:c.1124-81G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001079817.3:c.1124-81G>T - intron variant - [Sequence Ontology: SO:0001627]