Canonical Allele Identifier: CA59498028

Gene:

Linked Data

• dbSNP Id: rs952456846
• MyVariant Identifiers: chr2:g.161757172G>A (hg19) ; chr2:g.160900661G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.160900661G>A , CM000664.2:g.160900661G>A	GRCh38
NC_000002.11:g.161757172G>A , CM000664.1:g.161757172G>A	GRCh37
NC_000002.10:g.161465418G>A	NCBI36