Canonical Allele Identifier: CA185688669
Gene:

Linked Data

dbSNP Id: rs1001822770

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999532T>A , CM000670.2:g.126999532T>A GRCh38
NC_000008.10:g.128011777T>A , CM000670.1:g.128011777T>A GRCh37
NC_000008.9:g.128080959T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7023T>A