Canonical Allele Identifier: CA10654446

Gene:

Linked Data

• ClinVar Variation Id: 368878
• ClinVar RCV Id: RCV000315074
• dbSNP Id: rs6683669
• gnomAD v2: 1-59041092-G-A
• gnomAD v3: 1-58575420-G-A
• gnomAD v4: 1-58575420-G-A
• MyVariant Identifiers: chr1:g.59041092G>A (hg19) ; chr1:g.58575420G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58575420G>A , CM000663.2:g.58575420G>A	GRCh38
NC_000001.10:g.59041092G>A , CM000663.1:g.59041092G>A	GRCh37
NC_000001.9:g.58813680G>A	NCBI36
NG_016237.1:g.7075C>T