Canonical Allele Identifier: CA1216113097
Gene:

Linked Data

dbSNP Id: rs10737621

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121735C>G , CM000663.2:g.193121735C>G GRCh38
NC_000001.10:g.193090865C>G , CM000663.1:g.193090865C>G GRCh37
NC_000001.9:g.191357488C>G NCBI36
NG_012691.1:g.4778C>G , LRG_507:g.4778C>G

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1922G>C