Canonical Allele Identifier: CA2677040481

Gene: IRF4

Linked Data

• gnomAD v4: 6-395967-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.395967C>G , CM000668.2:g.395967C>G	GRCh38
NC_000006.11:g.395967C>G , CM000668.1:g.395967C>G	GRCh37
NC_000006.10:g.340967C>G	NCBI36
NG_027728.1:g.9229C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469834.2:n.612C>G
ENST00000493114.2:c.492+32C>G	ENSP00000436094.2:n.492+32C>G
ENST00000696871.1:c.492+32C>G	ENSP00000512940.1:n.492+32C>G
ENST00000696872.1:c.552+32C>G	ENSP00000512941.1:n.552+32C>G
ENST00000696873.1:c.57+32C>G	ENSP00000512942.1:n.57+32C>G
ENST00000380956.9:c.492+32C>G MANE Select	ENSP00000370343.4:n.492+32C>G
ENST00000380956.8:c.492+32C>G	ENSP00000370343.4:n.492+32C>G
ENST00000468485.5:n.366C>G
ENST00000493114.1:c.492+32C>G	ENSP00000436094.1:n.492+32C>G
ENST00000495137.5:n.318+32C>G
NM_001195286.1:c.492+32C>G	NP_001182215.1:n.492+32C>G
NM_002460.3:c.492+32C>G	NP_002451.2:n.492+32C>G
NR_046000.2:n.618+32C>G
XM_006715090.1:c.492+32C>G	XP_006715153.1:n.492+32C>G
XM_006715090.2:c.492+32C>G	XP_006715153.1:n.492+32C>G
NM_002460.4:c.492+32C>G MANE Select	NP_002451.2:n.492+32C>G
NM_001195286.2:c.492+32C>G	NP_001182215.1:n.492+32C>G
NR_046000.3:n.605+32C>G