Canonical Allele Identifier: CA1267947215
Gene:

Linked Data

dbSNP Id: rs137942127

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016011G>C , CM000664.2:g.88016011G>C GRCh38
NC_000002.11:g.88315530G>C , CM000664.1:g.88315530G>C GRCh37
NC_000002.10:g.88096645G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.356G>C
XR_940336.3:n.356G>C