Canonical Allele Identifier: CA2652992707
Gene: ADA HGNC NCBI

Linked Data

gnomAD v4: 20-44651941-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651941T>G , CM000682.2:g.44651941T>G GRCh38
NC_000020.10:g.43280582T>G , CM000682.1:g.43280582T>G GRCh37
NC_000020.9:g.42713996T>G NCBI36
NG_007385.1:g.4795A>C , LRG_16:g.4795A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-160A>C ENSP00000512234.1:n.-160A>C
ENST00000696039.1:n.282A>C
ENST00000696062.1:c.96+159A>C ENSP00000512365.1:n.96+159A>C
ENST00000696064.1:c.-157A>C ENSP00000512367.1:n.-157A>C
ENST00000535573.1:n.293A>C
ENST00000536076.1:n.174A>C
XM_011528479.1:c.-296A>C XP_011526781.1:n.-296A>C
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