Canonical Allele Identifier: CA2652992708

Gene: ADA

Linked Data

• gnomAD v4: 20-44651942-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651942T>C , CM000682.2:g.44651942T>C	GRCh38
NC_000020.10:g.43280583T>C , CM000682.1:g.43280583T>C	GRCh37
NC_000020.9:g.42713997T>C	NCBI36
NG_007385.1:g.4794A>G , LRG_16:g.4794A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-161A>G	ENSP00000512234.1:n.-161A>G
ENST00000696039.1:n.281A>G
ENST00000696062.1:c.96+158A>G	ENSP00000512365.1:n.96+158A>G
ENST00000696064.1:c.-158A>G	ENSP00000512367.1:n.-158A>G
ENST00000535573.1:n.292A>G
ENST00000536076.1:n.173A>G
XM_011528479.1:c.-297A>G	XP_011526781.1:n.-297A>G