Canonical Allele Identifier: CA2652992537
Gene: ADA HGNC NCBI

Linked Data

gnomAD v4: 20-44651803-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651803G>T , CM000682.2:g.44651803G>T GRCh38
NC_000020.10:g.43280444G>T , CM000682.1:g.43280444G>T GRCh37
NC_000020.9:g.42713858G>T NCBI36
NG_007385.1:g.4933C>A , LRG_16:g.4933C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+99C>A ENSP00000512234.1:n.-121+99C>A
ENST00000696039.1:n.321+99C>A
ENST00000696062.1:c.96+297C>A ENSP00000512365.1:n.96+297C>A
ENST00000696064.1:c.-118+99C>A ENSP00000512367.1:n.-118+99C>A
ENST00000696065.1:c.-121+99C>A ENSP00000512368.1:n.-121+99C>A
ENST00000535573.1:n.332+99C>A
ENST00000536076.1:n.213+99C>A
XM_011528479.1:c.-257+99C>A XP_011526781.1:n.-257+99C>A
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