Canonical Allele Identifier: CA732182695

Gene:

Linked Data

• dbSNP Id: rs1391079472
• MyVariant Identifiers: chr1:g.225074722G>A (hg19) ; chr1:g.224887020G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.224887020G>A , CM000663.2:g.224887020G>A	GRCh38
NC_000001.10:g.225074722G>A , CM000663.1:g.225074722G>A	GRCh37
NC_000001.9:g.223141345G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_949207.1:n.66-2239C>T
XR_949207.2:n.63-2239C>T