Canonical Allele Identifier: CA1267947190
Gene:

Linked Data

dbSNP Id: rs1672669067

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015966A>C , CM000664.2:g.88015966A>C GRCh38
NC_000002.11:g.88315485A>C , CM000664.1:g.88315485A>C GRCh37
NC_000002.10:g.88096600A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.311A>C
XR_940336.3:n.311A>C