Canonical Allele Identifier: CA2652992732

Gene: ADA

Linked Data

• gnomAD v4: 20-44651966-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651966T>C , CM000682.2:g.44651966T>C	GRCh38
NC_000020.10:g.43280607T>C , CM000682.1:g.43280607T>C	GRCh37
NC_000020.9:g.42714021T>C	NCBI36
NG_007385.1:g.4770A>G , LRG_16:g.4770A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-185A>G	ENSP00000512234.1:n.-185A>G
ENST00000696039.1:n.257A>G
ENST00000696062.1:c.96+134A>G	ENSP00000512365.1:n.96+134A>G
ENST00000696064.1:c.-182A>G	ENSP00000512367.1:n.-182A>G
ENST00000535573.1:n.268A>G
ENST00000536076.1:n.149A>G
XM_011528479.1:c.-321A>G	XP_011526781.1:n.-321A>G