Canonical Allele Identifier: CA50663569

Gene:

Linked Data

• dbSNP Id: rs1048698271
• MyVariant Identifiers: chr2:g.76375549T>A (hg19) ; chr2:g.76148423T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.76148423T>A , CM000664.2:g.76148423T>A	GRCh38
NC_000002.11:g.76375549T>A , CM000664.1:g.76375549T>A	GRCh37
NC_000002.10:g.76229057T>A	NCBI36