Canonical Allele Identifier: CA15119391

Gene:

Linked Data

• dbSNP Id: rs3116651
• gnomAD v2: 1-159698485-C-T
• gnomAD v3: 1-159728695-C-T
• gnomAD v4: 1-159728695-C-T
• MyVariant Identifiers: chr1:g.159698485C>T (hg19) ; chr1:g.159728695C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159728695C>T , CM000663.2:g.159728695C>T	GRCh38
NC_000001.10:g.159698485C>T , CM000663.1:g.159698485C>T	GRCh37
NC_000001.9:g.157965109C>T	NCBI36