Canonical Allele Identifier: CA2652992629
Gene: ADA HGNC NCBI

Linked Data

gnomAD v4: 20-44651874-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651874C>T , CM000682.2:g.44651874C>T GRCh38
NC_000020.10:g.43280515C>T , CM000682.1:g.43280515C>T GRCh37
NC_000020.9:g.42713929C>T NCBI36
NG_007385.1:g.4862G>A , LRG_16:g.4862G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+28G>A ENSP00000512234.1:n.-121+28G>A
ENST00000696039.1:n.321+28G>A
ENST00000696062.1:c.96+226G>A ENSP00000512365.1:n.96+226G>A
ENST00000696064.1:c.-118+28G>A ENSP00000512367.1:n.-118+28G>A
ENST00000696065.1:c.-121+28G>A ENSP00000512368.1:n.-121+28G>A
ENST00000535573.1:n.332+28G>A
ENST00000536076.1:n.213+28G>A
XM_011528479.1:c.-257+28G>A XP_011526781.1:n.-257+28G>A
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