Canonical Allele Identifier: CA364276012

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587303A>C , CM000668.2:g.43587303A>C GRCh38
NC_000006.11:g.43555040A>C , CM000668.1:g.43555040A>C GRCh37
NC_000006.10:g.43663018A>C NCBI36
NG_009252.1:g.16163A>C , LRG_470:g.16163A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.304A>C (POLH) MANE Select ENSP00000361310.4:p.Ile102Leu
ENST00000372226.1:c.304A>C (POLH) ENSP00000361300.1:p.Ile102Leu
ENST00000372236.8:c.304A>C (POLH) ENSP00000361310.4:p.Ile102Leu
ENST00000443535.1:c.118A>C (POLH) ENSP00000405320.1:p.Ile40Leu
NM_001291969.1:c.118+4162A>C (POLH) NP_001278898.1:n.118+4162A>C
NM_001291970.1:c.304A>C (POLH) NP_001278899.1:p.Ile102Leu
NM_006502.2:c.304A>C , LRG_470t1:c.304A>C (POLH) NP_006493.1:p.Ile102Leu
XM_005249186.2:c.118A>C (POLH) XP_005249243.1:p.Ile40Leu
XM_011514698.1:c.118+4162A>C (POLH) XP_011513000.1:n.118+4162A>C
XM_005249186.4:c.118A>C (POLH) XP_005249243.1:p.Ile40Leu
XM_011514698.3:c.118+4162A>C (POLH) XP_011513000.1:n.118+4162A>C
XM_024446466.1:c.52A>C (POLH) XP_024302234.1:p.Ile18Leu
XM_024446467.1:c.-316A>C (POLH) XP_024302235.1:n.-316A>C
NM_001291969.2:c.118+4162A>C (POLH) NP_001278898.1:n.118+4162A>C
NM_001291970.2:c.304A>C (POLH) NP_001278899.1:p.Ile102Leu
NM_006502.3:c.304A>C (POLH) MANE Select NP_006493.1:p.Ile102Leu
NM_001318876.2:c.945+58032A>C (POLR1C) NP_001305805.1:n.945+58032A>C