Canonical Allele Identifier: CA2652992703
Gene: ADA HGNC NCBI

Linked Data

gnomAD v4: 20-44651939-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651939C>T , CM000682.2:g.44651939C>T GRCh38
NC_000020.10:g.43280580C>T , CM000682.1:g.43280580C>T GRCh37
NC_000020.9:g.42713994C>T NCBI36
NG_007385.1:g.4797G>A , LRG_16:g.4797G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-158G>A ENSP00000512234.1:n.-158G>A
ENST00000696039.1:n.284G>A
ENST00000696062.1:c.96+161G>A ENSP00000512365.1:n.96+161G>A
ENST00000696064.1:c.-155G>A ENSP00000512367.1:n.-155G>A
ENST00000535573.1:n.295G>A
ENST00000536076.1:n.176G>A
XM_011528479.1:c.-294G>A XP_011526781.1:n.-294G>A
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