Canonical Allele Identifier: CA3825564
Gene: POLR1C HGNC NCBI

Linked Data

dbSNP Id: rs762584743
gnomAD v2: 6-43488483-C-G
gnomAD v4: 6-43520745-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43520745C>G , CM000668.2:g.43520745C>G GRCh38
NC_000006.11:g.43488483C>G , CM000668.1:g.43488483C>G GRCh37
NC_000006.10:g.43596461C>G NCBI36
NG_028283.1:g.8707C>G
NG_028283.3:g.16044C>G
NG_051658.1:g.60331G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000607635.2:c.776C>G ENSP00000496683.1:p.Pro259Arg
ENST00000642195.1:c.776C>G MANE Select ENSP00000496044.1:p.Pro259Arg
ENST00000643341.1:c.776C>G ENSP00000496018.1:p.Pro259Arg
ENST00000643799.1:c.656-187C>G ENSP00000494529.1:n.656-187C>G
ENST00000645141.1:c.*387C>G ENSP00000496755.1:n.*387C>G
ENST00000646188.1:c.611C>G ENSP00000496001.1:p.Pro204Arg
ENST00000646433.1:c.776C>G ENSP00000494368.1:p.Pro259Arg
ENST00000646700.1:c.776C>G ENSP00000495521.1:p.Pro259Arg
ENST00000304004.7:c.776C>G ENSP00000307212.3:p.Pro259Arg
ENST00000372344.6:c.656-187C>G ENSP00000361419.2:n.656-187C>G
ENST00000372389.7:c.776C>G ENSP00000361465.3:p.Pro259Arg
ENST00000455605.2:n.1266C>G
ENST00000481352.6:n.1148C>G
NM_203290.2:c.776C>G NP_976035.1:p.Pro259Arg
XM_005249491.1:c.776C>G XP_005249548.1:p.Pro259Arg
XM_011515000.1:c.776C>G XP_011513302.1:p.Pro259Arg
NM_001318876.1:c.776C>G NP_001305805.1:p.Pro259Arg
NM_001363658.1:c.776C>G NP_001350587.1:p.Pro259Arg
NM_203290.3:c.776C>G NP_976035.1:p.Pro259Arg
NM_203290.4:c.776C>G MANE Select NP_976035.1:p.Pro259Arg
NM_001363658.2:c.776C>G NP_001350587.1:p.Pro259Arg
NM_001318876.2:c.776C>G NP_001305805.1:p.Pro259Arg