Canonical Allele Identifier: CA362547350
Gene: IRF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.395935G>C , CM000668.2:g.395935G>C GRCh38
NC_000006.11:g.395935G>C , CM000668.1:g.395935G>C GRCh37
NC_000006.10:g.340935G>C NCBI36
NG_027728.1:g.9197G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000469834.2:n.580G>C
ENST00000493114.2:c.492G>C ENSP00000436094.2:p.Gln164His
ENST00000696871.1:c.492G>C ENSP00000512940.1:p.Gln164His
ENST00000696872.1:c.552G>C ENSP00000512941.1:p.Gln184His
ENST00000696873.1:c.57G>C ENSP00000512942.1:p.Gln19His
ENST00000380956.9:c.492G>C MANE Select ENSP00000370343.4:p.Gln164His
ENST00000380956.8:c.492G>C ENSP00000370343.4:p.Gln164His
ENST00000468485.5:n.334G>C
ENST00000493114.1:c.492G>C ENSP00000436094.1:p.Gln164His
ENST00000495137.5:n.318G>C
NM_001195286.1:c.492G>C NP_001182215.1:p.Gln164His
NM_002460.3:c.492G>C NP_002451.2:p.Gln164His
NR_046000.2:n.618G>C
XM_006715090.1:c.492G>C XP_006715153.1:p.Gln164His
XM_006715090.2:c.492G>C XP_006715153.1:p.Gln164His
NM_002460.4:c.492G>C MANE Select NP_002451.2:p.Gln164His
NM_001195286.2:c.492G>C NP_001182215.1:p.Gln164His
NR_046000.3:n.605G>C