Canonical Allele Identifier: CA744696908
Gene: ADA HGNC NCBI

Linked Data

dbSNP Id: rs1423862964
gnomAD v4: 20-44651865-C-T
MyVariant Identifiers: chr20:g.43280506C>T (hg19) chr20:g.44651865C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651865C>T , CM000682.2:g.44651865C>T GRCh38
NC_000020.10:g.43280506C>T , CM000682.1:g.43280506C>T GRCh37
NC_000020.9:g.42713920C>T NCBI36
NG_007385.1:g.4871G>A , LRG_16:g.4871G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+37G>A ENSP00000512234.1:n.-121+37G>A
ENST00000696039.1:n.321+37G>A
ENST00000696062.1:c.96+235G>A ENSP00000512365.1:n.96+235G>A
ENST00000696064.1:c.-118+37G>A ENSP00000512367.1:n.-118+37G>A
ENST00000696065.1:c.-121+37G>A ENSP00000512368.1:n.-121+37G>A
ENST00000535573.1:n.332+37G>A
ENST00000536076.1:n.213+37G>A
XM_011528479.1:c.-257+37G>A XP_011526781.1:n.-257+37G>A
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