Canonical Allele Identifier: CA10899779

Gene:

Linked Data

• dbSNP Id: rs555151599
• gnomAD v2: 1-25297486-G-T
• gnomAD v3: 1-24970995-G-T
• gnomAD v4: 1-24970995-G-T
• MyVariant Identifiers: chr1:g.25297486G>T (hg19) ; chr1:g.25297486_25297500delinsTGTGTGTGTGAGCTT (hg19) ; chr1:g.24970995G>T (hg38) ; chr1:g.24970995_24971009delinsTGTGTGTGTGAGCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.24970995G>T , CM000663.2:g.24970995G>T	GRCh38
NC_000001.10:g.25297486G>T , CM000663.1:g.25297486G>T	GRCh37
NC_000001.9:g.25170073G>T	NCBI36