Canonical Allele Identifier: CA364276063

Linked Data

dbSNP Id: rs1353169318
gnomAD v2: 6-43555049-C-T
gnomAD v3: 6-43587312-C-T
gnomAD v4: 6-43587312-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587312C>T , CM000668.2:g.43587312C>T GRCh38
NC_000006.11:g.43555049C>T , CM000668.1:g.43555049C>T GRCh37
NC_000006.10:g.43663027C>T NCBI36
NG_009252.1:g.16172C>T , LRG_470:g.16172C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.313C>T (POLH) MANE Select ENSP00000361310.4:p.Arg105Cys
ENST00000372226.1:c.313C>T (POLH) ENSP00000361300.1:p.Arg105Cys
ENST00000372236.8:c.313C>T (POLH) ENSP00000361310.4:p.Arg105Cys
ENST00000443535.1:c.127C>T (POLH) ENSP00000405320.1:p.Arg43Cys
NM_001291969.1:c.118+4171C>T (POLH) NP_001278898.1:n.118+4171C>T
NM_001291970.1:c.313C>T (POLH) NP_001278899.1:p.Arg105Cys
NM_006502.2:c.313C>T , LRG_470t1:c.313C>T (POLH) NP_006493.1:p.Arg105Cys
XM_005249186.2:c.127C>T (POLH) XP_005249243.1:p.Arg43Cys
XM_011514698.1:c.118+4171C>T (POLH) XP_011513000.1:n.118+4171C>T
XM_005249186.4:c.127C>T (POLH) XP_005249243.1:p.Arg43Cys
XM_011514698.3:c.118+4171C>T (POLH) XP_011513000.1:n.118+4171C>T
XM_024446466.1:c.61C>T (POLH) XP_024302234.1:p.Arg21Cys
XM_024446467.1:c.-307C>T (POLH) XP_024302235.1:n.-307C>T
NM_001291969.2:c.118+4171C>T (POLH) NP_001278898.1:n.118+4171C>T
NM_001291970.2:c.313C>T (POLH) NP_001278899.1:p.Arg105Cys
NM_006502.3:c.313C>T (POLH) MANE Select NP_006493.1:p.Arg105Cys
NM_001318876.2:c.945+58041C>T (POLR1C) NP_001305805.1:n.945+58041C>T