Canonical Allele Identifier: CA771173346

Gene:

Linked Data

• dbSNP Id: rs1442516434
• MyVariant Identifiers: chr2:g.646621A>C (hg19) ; chr2:g.646621A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.646621A>C , CM000664.2:g.646621A>C	GRCh38
NC_000002.11:g.646621A>C , CM000664.1:g.646621A>C	GRCh37
NC_000002.10:g.636621A>C	NCBI36