Canonical Allele Identifier: CA2652992684
Gene: ADA HGNC NCBI

Linked Data

gnomAD v4: 20-44651920-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651920G>T , CM000682.2:g.44651920G>T GRCh38
NC_000020.10:g.43280561G>T , CM000682.1:g.43280561G>T GRCh37
NC_000020.9:g.42713975G>T NCBI36
NG_007385.1:g.4816C>A , LRG_16:g.4816C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-139C>A ENSP00000512234.1:n.-139C>A
ENST00000696039.1:n.303C>A
ENST00000696062.1:c.96+180C>A ENSP00000512365.1:n.96+180C>A
ENST00000696064.1:c.-136C>A ENSP00000512367.1:n.-136C>A
ENST00000535573.1:n.314C>A
ENST00000536076.1:n.195C>A
XM_011528479.1:c.-275C>A XP_011526781.1:n.-275C>A
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