Canonical Allele Identifier: CA894254604

Gene:

Linked Data

• dbSNP Id: rs574022428
• gnomAD v3: 2-88016311-T-A
• gnomAD v4: 2-88016311-T-A
• MyVariant Identifiers: chr2:g.88315830T>A (hg19) ; chr2:g.88016311T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016311T>A , CM000664.2:g.88016311T>A	GRCh38
NC_000002.11:g.88315830T>A , CM000664.1:g.88315830T>A	GRCh37
NC_000002.10:g.88096945T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.656T>A
XR_940336.3:n.656T>A