Canonical Allele Identifier: CA364276043

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587308G>T , CM000668.2:g.43587308G>T GRCh38
NC_000006.11:g.43555045G>T , CM000668.1:g.43555045G>T GRCh37
NC_000006.10:g.43663023G>T NCBI36
NG_009252.1:g.16168G>T , LRG_470:g.16168G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.309G>T (POLH) MANE Select ENSP00000361310.4:p.Met103Ile
ENST00000372226.1:c.309G>T (POLH) ENSP00000361300.1:p.Met103Ile
ENST00000372236.8:c.309G>T (POLH) ENSP00000361310.4:p.Met103Ile
ENST00000443535.1:c.123G>T (POLH) ENSP00000405320.1:p.Met41Ile
NM_001291969.1:c.118+4167G>T (POLH) NP_001278898.1:n.118+4167G>T
NM_001291970.1:c.309G>T (POLH) NP_001278899.1:p.Met103Ile
NM_006502.2:c.309G>T , LRG_470t1:c.309G>T (POLH) NP_006493.1:p.Met103Ile
XM_005249186.2:c.123G>T (POLH) XP_005249243.1:p.Met41Ile
XM_011514698.1:c.118+4167G>T (POLH) XP_011513000.1:n.118+4167G>T
XM_005249186.4:c.123G>T (POLH) XP_005249243.1:p.Met41Ile
XM_011514698.3:c.118+4167G>T (POLH) XP_011513000.1:n.118+4167G>T
XM_024446466.1:c.57G>T (POLH) XP_024302234.1:p.Met19Ile
XM_024446467.1:c.-311G>T (POLH) XP_024302235.1:n.-311G>T
NM_001291969.2:c.118+4167G>T (POLH) NP_001278898.1:n.118+4167G>T
NM_001291970.2:c.309G>T (POLH) NP_001278899.1:p.Met103Ile
NM_006502.3:c.309G>T (POLH) MANE Select NP_006493.1:p.Met103Ile
NM_001318876.2:c.945+58037G>T (POLR1C) NP_001305805.1:n.945+58037G>T