Canonical Allele Identifier: CA364276325

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587363A>T , CM000668.2:g.43587363A>T GRCh38
NC_000006.11:g.43555100A>T , CM000668.1:g.43555100A>T GRCh37
NC_000006.10:g.43663078A>T NCBI36
NG_009252.1:g.16223A>T , LRG_470:g.16223A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.364A>T (POLH) MANE Select ENSP00000361310.4:p.Thr122Ser
ENST00000372226.1:c.364A>T (POLH) ENSP00000361300.1:p.Thr122Ser
ENST00000372236.8:c.364A>T (POLH) ENSP00000361310.4:p.Thr122Ser
ENST00000443535.1:c.178A>T (POLH) ENSP00000405320.1:p.Thr60Ser
NM_001291969.1:c.118+4222A>T (POLH) NP_001278898.1:n.118+4222A>T
NM_001291970.1:c.364A>T (POLH) NP_001278899.1:p.Thr122Ser
NM_006502.2:c.364A>T , LRG_470t1:c.364A>T (POLH) NP_006493.1:p.Thr122Ser
XM_005249186.2:c.178A>T (POLH) XP_005249243.1:p.Thr60Ser
XM_011514698.1:c.118+4222A>T (POLH) XP_011513000.1:n.118+4222A>T
XM_005249186.4:c.178A>T (POLH) XP_005249243.1:p.Thr60Ser
XM_011514698.3:c.118+4222A>T (POLH) XP_011513000.1:n.118+4222A>T
XM_024446466.1:c.112A>T (POLH) XP_024302234.1:p.Thr38Ser
XM_024446467.1:c.-256A>T (POLH) XP_024302235.1:n.-256A>T
NM_001291969.2:c.118+4222A>T (POLH) NP_001278898.1:n.118+4222A>T
NM_001291970.2:c.364A>T (POLH) NP_001278899.1:p.Thr122Ser
NM_006502.3:c.364A>T (POLH) MANE Select NP_006493.1:p.Thr122Ser
NM_001318876.2:c.945+58092A>T (POLR1C) NP_001305805.1:n.945+58092A>T