Canonical Allele Identifier: CA12194496

Gene:

Linked Data

• ClinVar Variation Id: 1278437
• ClinVar RCV Id: RCV001688045
• dbSNP Id: rs2275913
• gnomAD v2: 6-52051033-G-A
• gnomAD v3: 6-52186235-G-A
• gnomAD v4: 6-52186235-G-A
• MyVariant Identifiers: chr6:g.52051033G>A (hg19) ; chr6:g.52186235G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52186235G>A , CM000668.2:g.52186235G>A	GRCh38
NC_000006.11:g.52051033G>A , CM000668.1:g.52051033G>A	GRCh37
NC_000006.10:g.52158992G>A	NCBI36
NG_033021.1:g.4849G>A