Canonical Allele Identifier: CA2652992721

Gene: ADA

Linked Data

• gnomAD v4: 20-44651954-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651954C>T , CM000682.2:g.44651954C>T	GRCh38
NC_000020.10:g.43280595C>T , CM000682.1:g.43280595C>T	GRCh37
NC_000020.9:g.42714009C>T	NCBI36
NG_007385.1:g.4782G>A , LRG_16:g.4782G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-173G>A	ENSP00000512234.1:n.-173G>A
ENST00000696039.1:n.269G>A
ENST00000696062.1:c.96+146G>A	ENSP00000512365.1:n.96+146G>A
ENST00000696064.1:c.-170G>A	ENSP00000512367.1:n.-170G>A
ENST00000535573.1:n.280G>A
ENST00000536076.1:n.161G>A
XM_011528479.1:c.-309G>A	XP_011526781.1:n.-309G>A