Canonical Allele Identifier: CA700072776

Gene:

Linked Data

• dbSNP Id: rs1178951854
• MyVariant Identifiers: chr13:g.66120806A>T (hg19) ; chr13:g.65546674A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.65546674A>T , CM000675.2:g.65546674A>T	GRCh38
NC_000013.10:g.66120806A>T , CM000675.1:g.66120806A>T	GRCh37
NC_000013.9:g.65018807A>T	NCBI36