Canonical Allele Identifier: CA1267947203
Gene:

Linked Data

dbSNP Id: rs1672669549

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015991A>C , CM000664.2:g.88015991A>C GRCh38
NC_000002.11:g.88315510A>C , CM000664.1:g.88315510A>C GRCh37
NC_000002.10:g.88096625A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.336A>C
XR_940336.3:n.336A>C