Canonical Allele Identifier: CA2652992747
Gene: ADA HGNC NCBI

Linked Data

gnomAD v4: 20-44651984-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651984T>G , CM000682.2:g.44651984T>G GRCh38
NC_000020.10:g.43280625T>G , CM000682.1:g.43280625T>G GRCh37
NC_000020.9:g.42714039T>G NCBI36
NG_007385.1:g.4752A>C , LRG_16:g.4752A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-203A>C ENSP00000512234.1:n.-203A>C
ENST00000696039.1:n.239A>C
ENST00000696062.1:c.96+116A>C ENSP00000512365.1:n.96+116A>C
ENST00000696064.1:c.-200A>C ENSP00000512367.1:n.-200A>C
ENST00000535573.1:n.250A>C
ENST00000536076.1:n.131A>C
XM_011528479.1:c.-339A>C XP_011526781.1:n.-339A>C
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