Canonical Allele Identifier: CA744696879
Gene: ADA HGNC NCBI

Linked Data

dbSNP Id: rs1233965404
gnomAD v3: 20-44651802-C-T
gnomAD v4: 20-44651802-C-T
MyVariant Identifiers: chr20:g.43280443C>T (hg19) chr20:g.44651802C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651802C>T , CM000682.2:g.44651802C>T GRCh38
NC_000020.10:g.43280443C>T , CM000682.1:g.43280443C>T GRCh37
NC_000020.9:g.42713857C>T NCBI36
NG_007385.1:g.4934G>A , LRG_16:g.4934G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-121+100G>A ENSP00000512234.1:n.-121+100G>A
ENST00000696039.1:n.321+100G>A
ENST00000696062.1:c.96+298G>A ENSP00000512365.1:n.96+298G>A
ENST00000696064.1:c.-118+100G>A ENSP00000512367.1:n.-118+100G>A
ENST00000696065.1:c.-121+100G>A ENSP00000512368.1:n.-121+100G>A
ENST00000535573.1:n.332+100G>A
ENST00000536076.1:n.213+100G>A
XM_011528479.1:c.-257+100G>A XP_011526781.1:n.-257+100G>A
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