Canonical Allele Identifier: CA49004126

Gene:

Linked Data

• dbSNP Id: rs1038941791
• MyVariant Identifiers: chr2:g.60584834C>A (hg19) ; chr2:g.60357699C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60357699C>A , CM000664.2:g.60357699C>A	GRCh38
NC_000002.11:g.60584834C>A , CM000664.1:g.60584834C>A	GRCh37
NC_000002.10:g.60438338C>A	NCBI36