Canonical Allele Identifier: CA635985524
Gene: ADA HGNC NCBI

Linked Data

dbSNP Id: rs929584843

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651977C>G , CM000682.2:g.44651977C>G GRCh38
NC_000020.10:g.43280618C>G , CM000682.1:g.43280618C>G GRCh37
NC_000020.9:g.42714032C>G NCBI36
NG_007385.1:g.4759G>C , LRG_16:g.4759G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-196G>C ENSP00000512234.1:n.-196G>C
ENST00000696039.1:n.246G>C
ENST00000696062.1:c.96+123G>C ENSP00000512365.1:n.96+123G>C
ENST00000696064.1:c.-193G>C ENSP00000512367.1:n.-193G>C
ENST00000535573.1:n.257G>C
ENST00000536076.1:n.138G>C
XM_011528479.1:c.-332G>C XP_011526781.1:n.-332G>C