Canonical Allele Identifier: CA894254150

Gene:

Linked Data

• dbSNP Id: rs1334024654
• MyVariant Identifiers: chr2:g.88315610A>G (hg19) ; chr2:g.88016091A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016091A>G , CM000664.2:g.88016091A>G	GRCh38
NC_000002.11:g.88315610A>G , CM000664.1:g.88315610A>G	GRCh37
NC_000002.10:g.88096725A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.436A>G
XR_940336.3:n.436A>G