Canonical Allele Identifier: CA36909028

Gene:

Linked Data

• dbSNP Id: rs1000306956
• gnomAD v2: 1-208757406-C-T
• gnomAD v3: 1-208584061-C-T
• gnomAD v4: 1-208584061-C-T
• MyVariant Identifiers: chr1:g.208757406C>T (hg19) ; chr1:g.208584061C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.208584061C>T , CM000663.2:g.208584061C>T	GRCh38
NC_000001.10:g.208757406C>T , CM000663.1:g.208757406C>T	GRCh37
NC_000001.9:g.206824029C>T	NCBI36