Canonical Allele Identifier: CA3825507
Gene: POLR1C HGNC NCBI

Linked Data

ClinVar Variation Id: 2304761
ClinVar RCV Id: RCV002883792
dbSNP Id: rs765894120
gnomAD v2: 6-43488130-A-C
gnomAD v3: 6-43520392-A-C
gnomAD v4: 6-43520392-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43520392A>C , CM000668.2:g.43520392A>C GRCh38
NC_000006.11:g.43488130A>C , CM000668.1:g.43488130A>C GRCh37
NC_000006.10:g.43596108A>C NCBI36
NG_028283.1:g.8354A>C
NG_028283.3:g.15691A>C
NG_051658.1:g.60684T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.620A>C ENSP00000496683.1:p.Glu207Ala
ENST00000642195.1:c.620A>C MANE Select ENSP00000496044.1:p.Glu207Ala
ENST00000643341.1:c.620A>C ENSP00000496018.1:p.Glu207Ala
ENST00000643799.1:c.620A>C ENSP00000494529.1:p.Glu207Ala
ENST00000645141.1:c.*231A>C ENSP00000496755.1:n.*231A>C
ENST00000646188.1:c.455A>C ENSP00000496001.1:p.Glu152Ala
ENST00000646433.1:c.620A>C ENSP00000494368.1:p.Glu207Ala
ENST00000646700.1:c.620A>C ENSP00000495521.1:p.Glu207Ala
ENST00000304004.7:c.620A>C ENSP00000307212.3:p.Glu207Ala
ENST00000372344.6:c.620A>C ENSP00000361419.2:p.Glu207Ala
ENST00000372389.7:c.620A>C ENSP00000361465.3:p.Glu207Ala
ENST00000455605.2:n.913A>C
ENST00000481352.6:n.992A>C
ENST00000488601.6:n.859A>C
NM_203290.2:c.620A>C NP_976035.1:p.Glu207Ala
XM_005249491.1:c.620A>C XP_005249548.1:p.Glu207Ala
XM_011515000.1:c.620A>C XP_011513302.1:p.Glu207Ala
NM_001318876.1:c.620A>C NP_001305805.1:p.Glu207Ala
NM_001363658.1:c.620A>C NP_001350587.1:p.Glu207Ala
NM_203290.3:c.620A>C NP_976035.1:p.Glu207Ala
NM_203290.4:c.620A>C MANE Select NP_976035.1:p.Glu207Ala
NM_001363658.2:c.620A>C NP_001350587.1:p.Glu207Ala
NM_001318876.2:c.620A>C NP_001305805.1:p.Glu207Ala