Canonical Allele Identifier: CA744010571

Gene:

Linked Data

• dbSNP Id: rs512625
• MyVariant Identifiers: chr20:g.3648378A>T (hg19) ; chr20:g.3667731A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3667731A>T , CM000682.2:g.3667731A>T	GRCh38
NC_000020.10:g.3648378A>T , CM000682.1:g.3648378A>T	GRCh37
NC_000020.9:g.3596378A>T	NCBI36