Canonical Allele Identifier: CA427349457

Gene:

Linked Data

• dbSNP Id: rs886077354
• gnomAD v3: 2-88016398-C-A
• gnomAD v4: 2-88016398-C-A
• MyVariant Identifiers: chr2:g.88315917C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016398C>A , CM000664.2:g.88016398C>A	GRCh38
NC_000002.11:g.88315917C>A , CM000664.1:g.88315917C>A	GRCh37
NC_000002.10:g.88097032C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.743C>A
XR_940336.3:n.743C>A