Canonical Allele Identifier: CA1127875709
Gene:

Linked Data

dbSNP Id: rs1587835257

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092887A>G , CM000671.2:g.108092887A>G GRCh38
NC_000009.11:g.110855168A>G , CM000671.1:g.110855168A>G GRCh37
NC_000009.10:g.109894989A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930239.1:n.461-39593T>C
XR_001746881.1:n.668-39593T>C
XR_001746882.1:n.668-39593T>C