Canonical Allele Identifier: CA2365869177
Gene: ADA HGNC NCBI

Linked Data

dbSNP Id: rs2065652206
gnomAD v4: 20-44651944-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651944C>T , CM000682.2:g.44651944C>T GRCh38
NC_000020.10:g.43280585C>T , CM000682.1:g.43280585C>T GRCh37
NC_000020.9:g.42713999C>T NCBI36
NG_007385.1:g.4792G>A , LRG_16:g.4792G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-163G>A ENSP00000512234.1:n.-163G>A
ENST00000696039.1:n.279G>A
ENST00000696062.1:c.96+156G>A ENSP00000512365.1:n.96+156G>A
ENST00000696064.1:c.-160G>A ENSP00000512367.1:n.-160G>A
ENST00000535573.1:n.290G>A
ENST00000536076.1:n.171G>A
XM_011528479.1:c.-299G>A XP_011526781.1:n.-299G>A
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