Canonical Allele Identifier: CA136866012
Gene:

Linked Data

ClinVar Variation Id: 12387
ClinVar RCV Id: RCV000013188
dbSNP Id: rs1800750
gnomAD v2: 6-31542963-G-A
gnomAD v3: 6-31575186-G-A
gnomAD v4: 6-31575186-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31575186G>A , CM000668.2:g.31575186G>A GRCh38
NC_000006.11:g.31542963G>A , CM000668.1:g.31542963G>A GRCh37
NC_000006.10:g.31650942G>A NCBI36
NG_007462.1:g.4614G>A
NG_012010.1:g.8088G>A