Canonical Allele Identifier: CA13612647
Gene:

Linked Data

ClinVar Variation Id: 672938
ClinVar RCV Id: RCV000832200
dbSNP Id: rs2234649
gnomAD v2: 12-6451363-T-G
gnomAD v3: 12-6342197-T-G
gnomAD v4: 12-6342197-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6342197T>G , CM000674.2:g.6342197T>G GRCh38
NC_000012.11:g.6451363T>G , CM000674.1:g.6451363T>G GRCh37
NC_000012.10:g.6321624T>G NCBI36
NG_007506.1:g.4899A>C , LRG_193:g.4899A>C