Canonical Allele Identifier: CA913668202
Gene:

Linked Data

dbSNP Id: rs757519745

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128870973G>C , CM000673.2:g.128870973G>C GRCh38
NC_000011.9:g.128740868G>C , CM000673.1:g.128740868G>C GRCh37
NC_000011.8:g.128246078G>C NCBI36
NG_009379.1:g.1401C>G

Transcript Alleles

HGVS Amino-acid Change
XR_948172.1:n.5938C>G
XR_948173.1:n.5627C>G