Canonical Allele Identifier: CA12266081
Gene:

Linked Data

ClinVar Variation Id: 12390
ClinVar RCV Id: RCV000013198
dbSNP Id: rs1800630
gnomAD v2: 6-31542476-C-A
gnomAD v3: 6-31574699-C-A
gnomAD v4: 6-31574699-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31574699C>A , CM000668.2:g.31574699C>A GRCh38
NC_000006.11:g.31542476C>A , CM000668.1:g.31542476C>A GRCh37
NC_000006.10:g.31650455C>A NCBI36
NG_007462.1:g.4127C>A
NG_012010.1:g.7601C>A