Canonical Allele Identifier: CA315457397
Gene: ADA HGNC NCBI

Linked Data

dbSNP Id: rs932505038

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44651951C>A , CM000682.2:g.44651951C>A GRCh38
NC_000020.10:g.43280592C>A , CM000682.1:g.43280592C>A GRCh37
NC_000020.9:g.42714006C>A NCBI36
NG_007385.1:g.4785G>T , LRG_16:g.4785G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000536076.2:c.-170G>T ENSP00000512234.1:n.-170G>T
ENST00000696039.1:n.272G>T
ENST00000696062.1:c.96+149G>T ENSP00000512365.1:n.96+149G>T
ENST00000696064.1:c.-167G>T ENSP00000512367.1:n.-167G>T
ENST00000535573.1:n.283G>T
ENST00000536076.1:n.164G>T
XM_011528479.1:c.-306G>T XP_011526781.1:n.-306G>T