Canonical Allele Identifier: CA2736983732

Gene: ADA

Linked Data

• dbSNP Id: rs2145367991

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651988G>A , CM000682.2:g.44651988G>A	GRCh38
NC_000020.10:g.43280629G>A , CM000682.1:g.43280629G>A	GRCh37
NC_000020.9:g.42714043G>A	NCBI36
NG_007385.1:g.4748C>T , LRG_16:g.4748C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-207C>T	ENSP00000512234.1:n.-207C>T
ENST00000696039.1:n.235C>T
ENST00000696062.1:c.96+112C>T	ENSP00000512365.1:n.96+112C>T
ENST00000696064.1:c.-204C>T	ENSP00000512367.1:n.-204C>T
ENST00000535573.1:n.246C>T
ENST00000536076.1:n.127C>T
XM_011528479.1:c.-343C>T	XP_011526781.1:n.-343C>T