Canonical Allele Identifier: CA15724144

Gene:

Linked Data

• ClinVar Variation Id: 675609
• ClinVar RCV Id: RCV000834974
• dbSNP Id: rs4149570
• gnomAD v2: 12-6451590-A-C
• gnomAD v3: 12-6342424-A-C
• gnomAD v4: 12-6342424-A-C
• MyVariant Identifiers: chr12:g.6451590A>C (hg19) ; chr12:g.6342424A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6342424A>C , CM000674.2:g.6342424A>C	GRCh38
NC_000012.11:g.6451590A>C , CM000674.1:g.6451590A>C	GRCh37
NC_000012.10:g.6321851A>C	NCBI36
NG_007506.1:g.4672T>G , LRG_193:g.4672T>G