Canonical Allele Identifier: CA12231313

Gene:

Linked Data

• ClinVar Variation Id: 1048804
• ClinVar RCV Id: RCV001354057
• dbSNP Id: rs361525
• gnomAD v2: 6-31543101-G-A
• gnomAD v3: 6-31575324-G-A
• gnomAD v4: 6-31575324-G-A
• MyVariant Identifiers: chr6:g.31543101G>A (hg19) ; chr6:g.31575324G>A (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31575324G>A , CM000668.2:g.31575324G>A	GRCh38
NC_000006.11:g.31543101G>A , CM000668.1:g.31543101G>A	GRCh37
NC_000006.10:g.31651080G>A	NCBI36
NG_007462.1:g.4752G>A
NG_012010.1:g.8226G>A