Canonical Allele Identifier: CA217298768
Gene:

Linked Data

ClinVar Variation Id: 1707204
ClinVar RCV Id: RCV002286120
dbSNP Id: rs573977383
gnomAD v2: 11-6411512-G-A
gnomAD v3: 11-6390282-G-A
gnomAD v4: 11-6390282-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390282G>A , CM000673.2:g.6390282G>A GRCh38
NC_000011.9:g.6411512G>A , CM000673.1:g.6411512G>A GRCh37
NC_000011.8:g.6368088G>A NCBI36
NG_011780.1:g.4858G>A