Canonical Allele Identifier: CA2652992741

Gene: ADA

Linked Data

• gnomAD v4: 20-44651973-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651973T>C , CM000682.2:g.44651973T>C	GRCh38
NC_000020.10:g.43280614T>C , CM000682.1:g.43280614T>C	GRCh37
NC_000020.9:g.42714028T>C	NCBI36
NG_007385.1:g.4763A>G , LRG_16:g.4763A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-192A>G	ENSP00000512234.1:n.-192A>G
ENST00000696039.1:n.250A>G
ENST00000696062.1:c.96+127A>G	ENSP00000512365.1:n.96+127A>G
ENST00000696064.1:c.-189A>G	ENSP00000512367.1:n.-189A>G
ENST00000535573.1:n.261A>G
ENST00000536076.1:n.142A>G
XM_011528479.1:c.-328A>G	XP_011526781.1:n.-328A>G