Canonical Allele Identifier: CA2652992688
Gene: ADA HGNC NCBI

Linked Data

gnomAD v4: 20-44651923-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651923G>T , CM000682.2:g.44651923G>T GRCh38
NC_000020.10:g.43280564G>T , CM000682.1:g.43280564G>T GRCh37
NC_000020.9:g.42713978G>T NCBI36
NG_007385.1:g.4813C>A , LRG_16:g.4813C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-142C>A ENSP00000512234.1:n.-142C>A
ENST00000696039.1:n.300C>A
ENST00000696062.1:c.96+177C>A ENSP00000512365.1:n.96+177C>A
ENST00000696064.1:c.-139C>A ENSP00000512367.1:n.-139C>A
ENST00000535573.1:n.311C>A
ENST00000536076.1:n.192C>A
XM_011528479.1:c.-278C>A XP_011526781.1:n.-278C>A
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