Canonical Allele Identifier: CA2715793883
Gene:

Linked Data

dbSNP Id: rs2116480023

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306298T>A , CM000669.2:g.124306298T>A GRCh38
NC_000007.13:g.123946352T>A , CM000669.1:g.123946352T>A GRCh37
NC_000007.12:g.123733588T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-180T>A