Canonical Allele Identifier: CA51878305

Gene:

Linked Data

• dbSNP Id: rs548608892
• gnomAD v2: 2-88315735-A-G
• gnomAD v3: 2-88016216-A-G
• gnomAD v4: 2-88016216-A-G
• MyVariant Identifiers: chr2:g.88315735A>G (hg19) ; chr2:g.88016216A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016216A>G , CM000664.2:g.88016216A>G	GRCh38
NC_000002.11:g.88315735A>G , CM000664.1:g.88315735A>G	GRCh37
NC_000002.10:g.88096850A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.561A>G
XR_940336.3:n.561A>G