Canonical Allele Identifier: CA725265962
Gene: IRF8 HGNC NCBI

Linked Data

dbSNP Id: rs8046526

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.85918029C>A , CM000678.2:g.85918029C>A GRCh38
NC_000016.9:g.85951635C>A , CM000678.1:g.85951635C>A GRCh37
NC_000016.8:g.84509136C>A NCBI36
NG_029333.1:g.23862C>A , LRG_294:g.23862C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000564803.6:c.602-388C>A ENSP00000456992.2:n.602-388C>A
ENST00000566369.2:c.448-2080C>A ENSP00000455048.2:n.448-2080C>A
ENST00000569607.2:c.-11-388C>A ENSP00000456395.2:n.-11-388C>A
ENST00000696884.1:c.*34-388C>A ENSP00000512951.1:n.*34-388C>A
ENST00000696885.1:c.*1080-388C>A ENSP00000512952.1:n.*1080-388C>A
ENST00000696886.1:n.2735-388C>A
ENST00000696887.1:c.602-388C>A ENSP00000512953.1:n.602-388C>A
ENST00000696890.1:n.549-388C>A
ENST00000268638.10:c.602-388C>A MANE Select ENSP00000268638.4:n.602-388C>A
ENST00000268638.9:c.602-388C>A ENSP00000268638.4:n.602-388C>A
ENST00000562492.5:c.-11-388C>A ENSP00000455452.1:n.-11-388C>A
ENST00000564803.5:c.602-388C>A ENSP00000456992.1:n.602-388C>A
ENST00000566369.1:c.276-2080C>A
ENST00000569145.5:c.-30-388C>A ENSP00000455760.1:n.-30-388C>A
ENST00000569607.1:c.-11-388C>A ENSP00000456395.1:n.-11-388C>A
NM_002163.2:c.602-388C>A , LRG_294t1:c.602-388C>A NP_002154.1:n.602-388C>A
XM_011523064.1:c.-11-388C>A XP_011521366.1:n.-11-388C>A
NM_001363907.1:c.632-388C>A NP_001350836.1:n.632-388C>A
NM_001363908.1:c.-11-388C>A NP_001350837.1:n.-11-388C>A
NM_002163.3:c.602-388C>A NP_002154.1:n.602-388C>A
NM_002163.4:c.602-388C>A MANE Select NP_002154.1:n.602-388C>A