Canonical Allele Identifier: CA48901885

Gene:

Linked Data

• dbSNP Id: rs975107429
• MyVariant Identifiers: chr2:g.59789401G>A (hg19) ; chr2:g.59562266G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.59562266G>A , CM000664.2:g.59562266G>A	GRCh38
NC_000002.11:g.59789401G>A , CM000664.1:g.59789401G>A	GRCh37
NC_000002.10:g.59642905G>A	NCBI36