Canonical Allele Identifier: CA2365869193

Gene: ADA

Linked Data

• dbSNP Id: rs576374963

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651976C>T , CM000682.2:g.44651976C>T	GRCh38
NC_000020.10:g.43280617C>T , CM000682.1:g.43280617C>T	GRCh37
NC_000020.9:g.42714031C>T	NCBI36
NG_007385.1:g.4760G>A , LRG_16:g.4760G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-195G>A	ENSP00000512234.1:n.-195G>A
ENST00000696039.1:n.247G>A
ENST00000696062.1:c.96+124G>A	ENSP00000512365.1:n.96+124G>A
ENST00000696064.1:c.-192G>A	ENSP00000512367.1:n.-192G>A
ENST00000535573.1:n.258G>A
ENST00000536076.1:n.139G>A
XM_011528479.1:c.-331G>A	XP_011526781.1:n.-331G>A