Canonical Allele Identifier: CA1085197794
Gene: IRF4 HGNC NCBI

Linked Data

dbSNP Id: rs1761257465
gnomAD v3: 6-396326-T-A
gnomAD v4: 6-396326-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.396326T>A , CM000668.2:g.396326T>A GRCh38
NC_000006.11:g.396326T>A , CM000668.1:g.396326T>A GRCh37
NC_000006.10:g.341326T>A NCBI36
NG_027728.1:g.9588T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000493114.2:c.492+391T>A ENSP00000436094.2:n.492+391T>A
ENST00000696871.1:c.492+391T>A ENSP00000512940.1:n.492+391T>A
ENST00000696872.1:c.552+391T>A ENSP00000512941.1:n.552+391T>A
ENST00000696873.1:c.57+391T>A ENSP00000512942.1:n.57+391T>A
ENST00000380956.9:c.492+391T>A MANE Select ENSP00000370343.4:n.492+391T>A
ENST00000380956.8:c.492+391T>A ENSP00000370343.4:n.492+391T>A
ENST00000493114.1:c.492+391T>A ENSP00000436094.1:n.492+391T>A
ENST00000495137.5:n.318+391T>A
NM_001195286.1:c.492+391T>A NP_001182215.1:n.492+391T>A
NM_002460.3:c.492+391T>A NP_002451.2:n.492+391T>A
NR_046000.2:n.618+391T>A
XM_006715090.1:c.492+391T>A XP_006715153.1:n.492+391T>A
XM_006715090.2:c.492+391T>A XP_006715153.1:n.492+391T>A
NM_002460.4:c.492+391T>A MANE Select NP_002451.2:n.492+391T>A
NM_001195286.2:c.492+391T>A NP_001182215.1:n.492+391T>A
NR_046000.3:n.605+391T>A