Canonical Allele Identifier: CA3713873
Gene:

Linked Data

ClinVar Variation Id: 225964
dbSNP Id: rs1800629

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31575254G>A , CM000668.2:g.31575254G>A GRCh38
NC_000006.11:g.31543031G>A , CM000668.1:g.31543031G>A GRCh37
NC_000006.10:g.31651010G>A NCBI36
NG_007462.1:g.4682G>A
NG_012010.1:g.8156G>A