Canonical Allele Identifier: CA1267947162
Gene:

Linked Data

dbSNP Id: rs1672664402

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015919T>A , CM000664.2:g.88015919T>A GRCh38
NC_000002.11:g.88315438T>A , CM000664.1:g.88315438T>A GRCh37
NC_000002.10:g.88096553T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.264T>A
XR_940336.3:n.264T>A