Canonical Allele Identifier: CA38657631

Gene:

Linked Data

• dbSNP Id: rs368062613
• MyVariant Identifiers: chr1:g.224256321A>G (hg19) ; chr1:g.224068619A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.224068619A>G , CM000663.2:g.224068619A>G	GRCh38
NC_000001.10:g.224256321A>G , CM000663.1:g.224256321A>G	GRCh37
NC_000001.9:g.222322944A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949173.1:n.385+965A>G
XR_001737824.1:n.242+965A>G