Canonical Allele Identifier: CA1118991871
Gene:

Linked Data

dbSNP Id: rs1814936601

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999539G>A , CM000670.2:g.126999539G>A GRCh38
NC_000008.10:g.128011784G>A , CM000670.1:g.128011784G>A GRCh37
NC_000008.9:g.128080966G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7016G>A