Canonical Allele Identifier: CA364276106

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587321G>A , CM000668.2:g.43587321G>A GRCh38
NC_000006.11:g.43555058G>A , CM000668.1:g.43555058G>A GRCh37
NC_000006.10:g.43663036G>A NCBI36
NG_009252.1:g.16181G>A , LRG_470:g.16181G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.322G>A (POLH) MANE Select ENSP00000361310.4:p.Val108Met
ENST00000372226.1:c.322G>A (POLH) ENSP00000361300.1:p.Val108Met
ENST00000372236.8:c.322G>A (POLH) ENSP00000361310.4:p.Val108Met
ENST00000443535.1:c.136G>A (POLH) ENSP00000405320.1:p.Val46Met
NM_001291969.1:c.118+4180G>A (POLH) NP_001278898.1:n.118+4180G>A
NM_001291970.1:c.322G>A (POLH) NP_001278899.1:p.Val108Met
NM_006502.2:c.322G>A , LRG_470t1:c.322G>A (POLH) NP_006493.1:p.Val108Met
XM_005249186.2:c.136G>A (POLH) XP_005249243.1:p.Val46Met
XM_011514698.1:c.118+4180G>A (POLH) XP_011513000.1:n.118+4180G>A
XM_005249186.4:c.136G>A (POLH) XP_005249243.1:p.Val46Met
XM_011514698.3:c.118+4180G>A (POLH) XP_011513000.1:n.118+4180G>A
XM_024446466.1:c.70G>A (POLH) XP_024302234.1:p.Val24Met
XM_024446467.1:c.-298G>A (POLH) XP_024302235.1:n.-298G>A
NM_001291969.2:c.118+4180G>A (POLH) NP_001278898.1:n.118+4180G>A
NM_001291970.2:c.322G>A (POLH) NP_001278899.1:p.Val108Met
NM_006502.3:c.322G>A (POLH) MANE Select NP_006493.1:p.Val108Met
NM_001318876.2:c.945+58050G>A (POLR1C) NP_001305805.1:n.945+58050G>A