Canonical Allele Identifier: CA2699734802
Gene:

Linked Data

dbSNP Id: rs1573064830

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016260A>C , CM000664.2:g.88016260A>C GRCh38
NC_000002.11:g.88315779A>C , CM000664.1:g.88315779A>C GRCh37
NC_000002.10:g.88096894A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.605A>C
XR_940336.3:n.605A>C