Canonical Allele Identifier: CA2365869154

Gene: ADA

Linked Data

• dbSNP Id: rs2065651721

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651914G>C , CM000682.2:g.44651914G>C	GRCh38
NC_000020.10:g.43280555G>C , CM000682.1:g.43280555G>C	GRCh37
NC_000020.9:g.42713969G>C	NCBI36
NG_007385.1:g.4822C>G , LRG_16:g.4822C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-133C>G	ENSP00000512234.1:n.-133C>G
ENST00000696039.1:n.309C>G
ENST00000696062.1:c.96+186C>G	ENSP00000512365.1:n.96+186C>G
ENST00000696064.1:c.-130C>G	ENSP00000512367.1:n.-130C>G
ENST00000696065.1:c.-133C>G	ENSP00000512368.1:n.-133C>G
ENST00000535573.1:n.320C>G
ENST00000536076.1:n.201C>G
XM_011528479.1:c.-269C>G	XP_011526781.1:n.-269C>G