Canonical Allele Identifier: CA126965
Gene:

Linked Data

ClinVar Variation Id: 16916
dbSNP Id: rs2740574

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99784473C>T , CM000669.2:g.99784473C>T GRCh38
NC_000007.13:g.99382096C>T , CM000669.1:g.99382096C>T GRCh37
NC_000007.12:g.99220032C>T NCBI36
NG_008421.1:g.4713G>A