Canonical Allele Identifier: CA2652992723
Gene: ADA HGNC NCBI

Linked Data

gnomAD v4: 20-44651955-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651955T>C , CM000682.2:g.44651955T>C GRCh38
NC_000020.10:g.43280596T>C , CM000682.1:g.43280596T>C GRCh37
NC_000020.9:g.42714010T>C NCBI36
NG_007385.1:g.4781A>G , LRG_16:g.4781A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-174A>G ENSP00000512234.1:n.-174A>G
ENST00000696039.1:n.268A>G
ENST00000696062.1:c.96+145A>G ENSP00000512365.1:n.96+145A>G
ENST00000696064.1:c.-171A>G ENSP00000512367.1:n.-171A>G
ENST00000535573.1:n.279A>G
ENST00000536076.1:n.160A>G
XM_011528479.1:c.-310A>G XP_011526781.1:n.-310A>G
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