Canonical Allele Identifier: CA1267947176
Gene:

Linked Data

dbSNP Id: rs1672668583

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015945C>A , CM000664.2:g.88015945C>A GRCh38
NC_000002.11:g.88315464C>A , CM000664.1:g.88315464C>A GRCh37
NC_000002.10:g.88096579C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.290C>A
XR_940336.3:n.290C>A