Canonical Allele Identifier: CA315457352

Gene: ADA

Linked Data

• dbSNP Id: rs978462381
• gnomAD v3: 20-44651909-C-T
• gnomAD v4: 20-44651909-C-T
• MyVariant Identifiers: chr20:g.43280550C>T (hg19) ; chr20:g.44651909C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651909C>T , CM000682.2:g.44651909C>T	GRCh38
NC_000020.10:g.43280550C>T , CM000682.1:g.43280550C>T	GRCh37
NC_000020.9:g.42713964C>T	NCBI36
NG_007385.1:g.4827G>A , LRG_16:g.4827G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-128G>A	ENSP00000512234.1:n.-128G>A
ENST00000696039.1:n.314G>A
ENST00000696062.1:c.96+191G>A	ENSP00000512365.1:n.96+191G>A
ENST00000696064.1:c.-125G>A	ENSP00000512367.1:n.-125G>A
ENST00000696065.1:c.-128G>A	ENSP00000512368.1:n.-128G>A
ENST00000535573.1:n.325G>A
ENST00000536076.1:n.206G>A
XM_011528479.1:c.-264G>A	XP_011526781.1:n.-264G>A