Canonical Allele Identifier: CA15137531

Gene:

Linked Data

• ClinVar Variation Id: 17936
• ClinVar RCV Id: RCV000019529
• dbSNP Id: rs5082
• gnomAD v2: 1-161193683-G-A
• gnomAD v3: 1-161223893-G-A
• gnomAD v4: 1-161223893-G-A
• MyVariant Identifiers: chr1:g.161193683G>A (hg19) ; chr1:g.161223893G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161223893G>A , CM000663.2:g.161223893G>A	GRCh38
NC_000001.10:g.161193683G>A , CM000663.1:g.161193683G>A	GRCh37
NC_000001.9:g.159460307G>A	NCBI36
NG_012043.1:g.4736C>T