Canonical Allele Identifier: CA364276053

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587310C>A , CM000668.2:g.43587310C>A GRCh38
NC_000006.11:g.43555047C>A , CM000668.1:g.43555047C>A GRCh37
NC_000006.10:g.43663025C>A NCBI36
NG_009252.1:g.16170C>A , LRG_470:g.16170C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.311C>A (POLH) MANE Select ENSP00000361310.4:p.Ser104Tyr
ENST00000372226.1:c.311C>A (POLH) ENSP00000361300.1:p.Ser104Tyr
ENST00000372236.8:c.311C>A (POLH) ENSP00000361310.4:p.Ser104Tyr
ENST00000443535.1:c.125C>A (POLH) ENSP00000405320.1:p.Ser42Tyr
NM_001291969.1:c.118+4169C>A (POLH) NP_001278898.1:n.118+4169C>A
NM_001291970.1:c.311C>A (POLH) NP_001278899.1:p.Ser104Tyr
NM_006502.2:c.311C>A , LRG_470t1:c.311C>A (POLH) NP_006493.1:p.Ser104Tyr
XM_005249186.2:c.125C>A (POLH) XP_005249243.1:p.Ser42Tyr
XM_011514698.1:c.118+4169C>A (POLH) XP_011513000.1:n.118+4169C>A
XM_005249186.4:c.125C>A (POLH) XP_005249243.1:p.Ser42Tyr
XM_011514698.3:c.118+4169C>A (POLH) XP_011513000.1:n.118+4169C>A
XM_024446466.1:c.59C>A (POLH) XP_024302234.1:p.Ser20Tyr
XM_024446467.1:c.-309C>A (POLH) XP_024302235.1:n.-309C>A
NM_001291969.2:c.118+4169C>A (POLH) NP_001278898.1:n.118+4169C>A
NM_001291970.2:c.311C>A (POLH) NP_001278899.1:p.Ser104Tyr
NM_006502.3:c.311C>A (POLH) MANE Select NP_006493.1:p.Ser104Tyr
NM_001318876.2:c.945+58039C>A (POLR1C) NP_001305805.1:n.945+58039C>A