Canonical Allele Identifier: CA2239538865

Gene: IRF8

Linked Data

• dbSNP Id: rs1905388256

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.85918322T>C , CM000678.2:g.85918322T>C	GRCh38
NC_000016.9:g.85951928T>C , CM000678.1:g.85951928T>C	GRCh37
NC_000016.8:g.84509429T>C	NCBI36
NG_029333.1:g.24155T>C , LRG_294:g.24155T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000564803.6:c.602-95T>C	ENSP00000456992.2:n.602-95T>C
ENST00000566369.2:c.448-1787T>C	ENSP00000455048.2:n.448-1787T>C
ENST00000569607.2:c.-11-95T>C	ENSP00000456395.2:n.-11-95T>C
ENST00000696884.1:c.*34-95T>C	ENSP00000512951.1:n.*34-95T>C
ENST00000696885.1:c.*1080-95T>C	ENSP00000512952.1:n.*1080-95T>C
ENST00000696886.1:n.2735-95T>C
ENST00000696887.1:c.602-95T>C	ENSP00000512953.1:n.602-95T>C
ENST00000696890.1:n.549-95T>C
ENST00000268638.10:c.602-95T>C MANE Select	ENSP00000268638.4:n.602-95T>C
ENST00000268638.9:c.602-95T>C	ENSP00000268638.4:n.602-95T>C
ENST00000562492.5:c.-11-95T>C	ENSP00000455452.1:n.-11-95T>C
ENST00000564803.5:c.602-95T>C	ENSP00000456992.1:n.602-95T>C
ENST00000566369.1:c.276-1787T>C
ENST00000569145.5:c.-30-95T>C	ENSP00000455760.1:n.-30-95T>C
ENST00000569607.1:c.-11-95T>C	ENSP00000456395.1:n.-11-95T>C
NM_002163.2:c.602-95T>C , LRG_294t1:c.602-95T>C	NP_002154.1:n.602-95T>C
XM_011523064.1:c.-11-95T>C	XP_011521366.1:n.-11-95T>C
NM_001363907.1:c.632-95T>C	NP_001350836.1:n.632-95T>C
NM_001363908.1:c.-11-95T>C	NP_001350837.1:n.-11-95T>C
NM_002163.3:c.602-95T>C	NP_002154.1:n.602-95T>C
NM_002163.4:c.602-95T>C MANE Select	NP_002154.1:n.602-95T>C