Canonical Allele Identifier: CA364276746

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587444G>C , CM000668.2:g.43587444G>C GRCh38
NC_000006.11:g.43555181G>C , CM000668.1:g.43555181G>C GRCh37
NC_000006.10:g.43663159G>C NCBI36
NG_009252.1:g.16304G>C , LRG_470:g.16304G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.445G>C (POLH) MANE Select ENSP00000361310.4:p.Gly149Arg
ENST00000372226.1:c.445G>C (POLH) ENSP00000361300.1:p.Gly149Arg
ENST00000372236.8:c.445G>C (POLH) ENSP00000361310.4:p.Gly149Arg
NM_001291969.1:c.118+4303G>C (POLH) NP_001278898.1:n.118+4303G>C
NM_001291970.1:c.445G>C (POLH) NP_001278899.1:p.Gly149Arg
NM_006502.2:c.445G>C , LRG_470t1:c.445G>C (POLH) NP_006493.1:p.Gly149Arg
XM_005249186.2:c.259G>C (POLH) XP_005249243.1:p.Gly87Arg
XM_011514698.1:c.118+4303G>C (POLH) XP_011513000.1:n.118+4303G>C
XM_005249186.4:c.259G>C (POLH) XP_005249243.1:p.Gly87Arg
XM_011514698.3:c.118+4303G>C (POLH) XP_011513000.1:n.118+4303G>C
XM_024446466.1:c.193G>C (POLH) XP_024302234.1:p.Gly65Arg
XM_024446467.1:c.-175G>C (POLH) XP_024302235.1:n.-175G>C
NM_001291969.2:c.118+4303G>C (POLH) NP_001278898.1:n.118+4303G>C
NM_001291970.2:c.445G>C (POLH) NP_001278899.1:p.Gly149Arg
NM_006502.3:c.445G>C (POLH) MANE Select NP_006493.1:p.Gly149Arg
NM_001318876.2:c.945+58173G>C (POLR1C) NP_001305805.1:n.945+58173G>C