Canonical Allele Identifier: CA2720412182
Gene:

Linked Data

dbSNP Id: rs2131348539

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.111236676T>A , CM000671.2:g.111236676T>A GRCh38
NC_000009.11:g.113998956T>A , CM000671.1:g.113998956T>A GRCh37
NC_000009.10:g.113038777T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930247.1:n.476+36137A>T
XR_930248.1:n.556+36137A>T
XR_930249.1:n.476+36137A>T
XR_001746893.1:n.476+36137A>T
XR_001746894.1:n.476+36137A>T
XR_930247.2:n.476+36137A>T