Canonical Allele Identifier: CA313629697
Gene:

Linked Data

dbSNP Id: rs928922347

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661638A>C , CM000682.2:g.23661638A>C GRCh38
NC_000020.10:g.23642275A>C , CM000682.1:g.23642275A>C GRCh37
NC_000020.9:g.23590275A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754712.1:n.268A>C