Canonical Allele Identifier: CA427349470

Gene:

Linked Data

• gnomAD v4: 2-88016405-T-A
• MyVariant Identifiers: chr2:g.88315924T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016405T>A , CM000664.2:g.88016405T>A	GRCh38
NC_000002.11:g.88315924T>A , CM000664.1:g.88315924T>A	GRCh37
NC_000002.10:g.88097039T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.750T>A
XR_940336.3:n.750T>A