Canonical Allele Identifier: CA6434517
Gene: AICDA HGNC NCBI

Linked Data

ClinVar Variation Id: 532543
ClinVar RCV Id: RCV000639379
dbSNP Id: rs61730095
gnomAD v2: 12-8759543-C-T
gnomAD v3: 12-8606947-C-T
gnomAD v4: 12-8606947-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8606947C>T , CM000674.2:g.8606947C>T GRCh38
NC_000012.11:g.8759543C>T , CM000674.1:g.8759543C>T GRCh37
NC_000012.10:g.8650810C>T NCBI36
NG_011588.1:g.10900G>A , LRG_17:g.10900G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.74G>A ENSP00000445691.1:p.Arg25His
ENST00000543081.6:c.74G>A ENSP00000439103.2:p.Arg25His
ENST00000544516.6:c.74G>A ENSP00000439538.2:p.Arg25His
ENST00000545576.2:n.183G>A
ENST00000696246.1:c.59G>A ENSP00000512504.1:p.Arg20His
ENST00000696271.1:n.194G>A
ENST00000696272.1:c.59G>A ENSP00000512515.1:p.Arg20His
ENST00000696273.1:c.107G>A ENSP00000512516.1:p.Arg36His
ENST00000229335.11:c.74G>A MANE Select ENSP00000229335.6:p.Arg25His
ENST00000229335.10:c.74G>A ENSP00000229335.6:p.Arg25His
ENST00000537228.5:c.74G>A ENSP00000445691.1:p.Arg25His
ENST00000543081.5:c.70G>A
ENST00000544516.5:c.70G>A
ENST00000545512.1:c.70G>A
ENST00000545576.1:n.108G>A
NM_020661.2:c.74G>A , LRG_17t1:c.74G>A NP_065712.1:p.Arg25His
XM_011520772.1:c.74G>A XP_011519074.1:p.Arg25His
XM_011520773.1:c.74G>A XP_011519075.1:p.Arg25His
NM_001330343.1:c.74G>A NP_001317272.1:p.Arg25His
NM_020661.3:c.74G>A NP_065712.1:p.Arg25His
XM_011520773.2:c.74G>A XP_011519075.1:p.Arg25His
NM_020661.4:c.74G>A MANE Select NP_065712.1:p.Arg25His
NM_001330343.2:c.74G>A NP_001317272.1:p.Arg25His