Canonical Allele Identifier: CA1085197696

Gene: IRF4

Linked Data

• dbSNP Id: rs1761242901
• gnomAD v3: 6-395961-T-C
• gnomAD v4: 6-395961-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.395961T>C , CM000668.2:g.395961T>C	GRCh38
NC_000006.11:g.395961T>C , CM000668.1:g.395961T>C	GRCh37
NC_000006.10:g.340961T>C	NCBI36
NG_027728.1:g.9223T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000469834.2:n.606T>C
ENST00000493114.2:c.492+26T>C	ENSP00000436094.2:n.492+26T>C
ENST00000696871.1:c.492+26T>C	ENSP00000512940.1:n.492+26T>C
ENST00000696872.1:c.552+26T>C	ENSP00000512941.1:n.552+26T>C
ENST00000696873.1:c.57+26T>C	ENSP00000512942.1:n.57+26T>C
ENST00000380956.9:c.492+26T>C MANE Select	ENSP00000370343.4:n.492+26T>C
ENST00000380956.8:c.492+26T>C	ENSP00000370343.4:n.492+26T>C
ENST00000468485.5:n.360T>C
ENST00000493114.1:c.492+26T>C	ENSP00000436094.1:n.492+26T>C
ENST00000495137.5:n.318+26T>C
NM_001195286.1:c.492+26T>C	NP_001182215.1:n.492+26T>C
NM_002460.3:c.492+26T>C	NP_002451.2:n.492+26T>C
NR_046000.2:n.618+26T>C
XM_006715090.1:c.492+26T>C	XP_006715153.1:n.492+26T>C
XM_006715090.2:c.492+26T>C	XP_006715153.1:n.492+26T>C
NM_002460.4:c.492+26T>C MANE Select	NP_002451.2:n.492+26T>C
NM_001195286.2:c.492+26T>C	NP_001182215.1:n.492+26T>C
NR_046000.3:n.605+26T>C