Canonical Allele Identifier: CA318813266

Gene:

Linked Data

• dbSNP Id: rs571905400
• MyVariant Identifiers: chr21:g.23631677T>A (hg19) ; chr21:g.22259357T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.22259357T>A , CM000683.2:g.22259357T>A	GRCh38
NC_000021.8:g.23631677T>A , CM000683.1:g.23631677T>A	GRCh37
NC_000021.7:g.22553548T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001754978.1:n.221+46544T>A