Canonical Allele Identifier: CA824571540

Gene: IRF4

Linked Data

• dbSNP Id: rs1161404258
• MyVariant Identifiers: chr6:g.396387C>G (hg19) ; chr6:g.396387C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.396387C>G , CM000668.2:g.396387C>G	GRCh38
NC_000006.11:g.396387C>G , CM000668.1:g.396387C>G	GRCh37
NC_000006.10:g.341387C>G	NCBI36
NG_027728.1:g.9649C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000493114.2:c.492+452C>G	ENSP00000436094.2:n.492+452C>G
ENST00000696871.1:c.492+452C>G	ENSP00000512940.1:n.492+452C>G
ENST00000696872.1:c.552+452C>G	ENSP00000512941.1:n.552+452C>G
ENST00000696873.1:c.57+452C>G	ENSP00000512942.1:n.57+452C>G
ENST00000380956.9:c.492+452C>G MANE Select	ENSP00000370343.4:n.492+452C>G
ENST00000380956.8:c.492+452C>G	ENSP00000370343.4:n.492+452C>G
ENST00000493114.1:c.492+452C>G	ENSP00000436094.1:n.492+452C>G
ENST00000495137.5:n.318+452C>G
NM_001195286.1:c.492+452C>G	NP_001182215.1:n.492+452C>G
NM_002460.3:c.492+452C>G	NP_002451.2:n.492+452C>G
NR_046000.2:n.618+452C>G
XM_006715090.1:c.492+452C>G	XP_006715153.1:n.492+452C>G
XM_006715090.2:c.492+452C>G	XP_006715153.1:n.492+452C>G
NM_002460.4:c.492+452C>G MANE Select	NP_002451.2:n.492+452C>G
NM_001195286.2:c.492+452C>G	NP_001182215.1:n.492+452C>G
NR_046000.3:n.605+452C>G