Canonical Allele Identifier: CA2652992737

Gene: ADA

Linked Data

• gnomAD v4: 20-44651971-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651971C>T , CM000682.2:g.44651971C>T	GRCh38
NC_000020.10:g.43280612C>T , CM000682.1:g.43280612C>T	GRCh37
NC_000020.9:g.42714026C>T	NCBI36
NG_007385.1:g.4765G>A , LRG_16:g.4765G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-190G>A	ENSP00000512234.1:n.-190G>A
ENST00000696039.1:n.252G>A
ENST00000696062.1:c.96+129G>A	ENSP00000512365.1:n.96+129G>A
ENST00000696064.1:c.-187G>A	ENSP00000512367.1:n.-187G>A
ENST00000535573.1:n.263G>A
ENST00000536076.1:n.144G>A
XM_011528479.1:c.-326G>A	XP_011526781.1:n.-326G>A