Canonical Allele Identifier: CA1835143
Gene: POLR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112564367G>C , CM000664.2:g.112564367G>C GRCh38
NC_000002.11:g.113321944G>C , CM000664.1:g.113321944G>C GRCh37
NC_000002.10:g.113038415G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000263331.10:c.1614G>C MANE Select ENSP00000263331.5:p.Gly538=
ENST00000263331.9:c.1614G>C ENSP00000263331.5:p.Gly538=
ENST00000333990.10:c.*1484G>C ENSP00000334589.6:n.*1484G>C
ENST00000409894.7:c.1160G>C ENSP00000387143.3:p.Gly387Ala
ENST00000417433.6:c.1446G>C ENSP00000405358.2:p.Gly482=
ENST00000448770.5:c.179G>C ENSP00000390274.1:p.Gly60Ala
ENST00000458012.2:c.6G>C ENSP00000394408.2:p.Gly2=
ENST00000484574.1:n.54G>C
ENST00000537335.5:c.981G>C ENSP00000437914.1:p.Gly327=
ENST00000541869.5:c.1728G>C ENSP00000444136.1:p.Gly576=
NM_001137604.2:c.1446G>C NP_001131076.1:p.Gly482=
NM_001282772.1:c.1728G>C NP_001269701.1:p.Gly576=
NM_001282774.1:c.1160G>C NP_001269703.1:p.Gly387Ala
NM_001282776.1:c.981G>C NP_001269705.1:p.Gly327=
NM_001282777.1:c.1197G>C NP_001269706.1:p.Gly399=
NM_001282779.1:c.1197G>C NP_001269708.1:p.Gly399=
NM_019014.5:c.1614G>C NP_061887.2:p.Gly538=
NM_001137604.3:c.1446G>C NP_001131076.1:p.Gly482=
NM_001282772.2:c.1728G>C NP_001269701.1:p.Gly576=
NM_001282774.2:c.1160G>C NP_001269703.1:p.Gly387Ala
NM_001282776.2:c.981G>C NP_001269705.1:p.Gly327=
NM_001282777.2:c.1197G>C NP_001269706.1:p.Gly399=
NM_001282779.2:c.1197G>C NP_001269708.1:p.Gly399=
NM_001371969.1:c.1614G>C NP_001358898.1:p.Gly538=
NM_001371970.1:c.1197G>C NP_001358899.1:p.Gly399=
NM_001371971.1:c.981G>C NP_001358900.1:p.Gly327=
NM_019014.6:c.1614G>C MANE Select NP_061887.2:p.Gly538=