Canonical Allele Identifier: CA49004128

Gene:

Linked Data

• dbSNP Id: rs1009616140
• MyVariant Identifiers: chr2:g.60584836A>T (hg19) ; chr2:g.60357701A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60357701A>T , CM000664.2:g.60357701A>T	GRCh38
NC_000002.11:g.60584836A>T , CM000664.1:g.60584836A>T	GRCh37
NC_000002.10:g.60438340A>T	NCBI36