Canonical Allele Identifier: CA1834910

Gene: POLR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112550939T>A , CM000664.2:g.112550939T>A	GRCh38
NC_000002.11:g.113308516T>A , CM000664.1:g.113308516T>A	GRCh37
NC_000002.10:g.113024987T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263331.10:c.699T>A MANE Select	ENSP00000263331.5:p.Thr233=
ENST00000263331.9:c.699T>A	ENSP00000263331.5:p.Thr233=
ENST00000333990.10:c.*569T>A	ENSP00000334589.6:n.*569T>A
ENST00000409894.7:c.699T>A	ENSP00000387143.3:p.Thr233=
ENST00000417433.6:c.531T>A	ENSP00000405358.2:p.Thr177=
ENST00000430293.1:c.*53T>A	ENSP00000403094.1:n.*53T>A
ENST00000448770.5:c.177+8268T>A	ENSP00000390274.1:n.177+8268T>A
ENST00000475318.1:n.233T>A
ENST00000537335.5:c.66T>A	ENSP00000437914.1:p.Thr22=
ENST00000541869.5:c.813T>A	ENSP00000444136.1:p.Thr271=
NM_001137604.2:c.531T>A	NP_001131076.1:p.Thr177=
NM_001282772.1:c.813T>A	NP_001269701.1:p.Thr271=
NM_001282774.1:c.699T>A	NP_001269703.1:p.Thr233=
NM_001282776.1:c.66T>A	NP_001269705.1:p.Thr22=
NM_001282777.1:c.282T>A	NP_001269706.1:p.Thr94=
NM_001282779.1:c.282T>A	NP_001269708.1:p.Thr94=
NM_019014.5:c.699T>A	NP_061887.2:p.Thr233=
NM_001137604.3:c.531T>A	NP_001131076.1:p.Thr177=
NM_001282772.2:c.813T>A	NP_001269701.1:p.Thr271=
NM_001282774.2:c.699T>A	NP_001269703.1:p.Thr233=
NM_001282776.2:c.66T>A	NP_001269705.1:p.Thr22=
NM_001282777.2:c.282T>A	NP_001269706.1:p.Thr94=
NM_001282779.2:c.282T>A	NP_001269708.1:p.Thr94=
NM_001371969.1:c.699T>A	NP_001358898.1:p.Thr233=
NM_001371970.1:c.282T>A	NP_001358899.1:p.Thr94=
NM_001371971.1:c.66T>A	NP_001358900.1:p.Thr22=
NM_019014.6:c.699T>A MANE Select	NP_061887.2:p.Thr233=