Canonical Allele Identifier: CA2365869196

Gene: ADA

Linked Data

• dbSNP Id: rs2065652626

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651978C>A , CM000682.2:g.44651978C>A	GRCh38
NC_000020.10:g.43280619C>A , CM000682.1:g.43280619C>A	GRCh37
NC_000020.9:g.42714033C>A	NCBI36
NG_007385.1:g.4758G>T , LRG_16:g.4758G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-197G>T	ENSP00000512234.1:n.-197G>T
ENST00000696039.1:n.245G>T
ENST00000696062.1:c.96+122G>T	ENSP00000512365.1:n.96+122G>T
ENST00000696064.1:c.-194G>T	ENSP00000512367.1:n.-194G>T
ENST00000535573.1:n.256G>T
ENST00000536076.1:n.137G>T
XM_011528479.1:c.-333G>T	XP_011526781.1:n.-333G>T