Canonical Allele Identifier: CA364276202

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587340T>G , CM000668.2:g.43587340T>G GRCh38
NC_000006.11:g.43555077T>G , CM000668.1:g.43555077T>G GRCh37
NC_000006.10:g.43663055T>G NCBI36
NG_009252.1:g.16200T>G , LRG_470:g.16200T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.341T>G (POLH) MANE Select ENSP00000361310.4:p.Ile114Ser
ENST00000372226.1:c.341T>G (POLH) ENSP00000361300.1:p.Ile114Ser
ENST00000372236.8:c.341T>G (POLH) ENSP00000361310.4:p.Ile114Ser
ENST00000443535.1:c.155T>G (POLH) ENSP00000405320.1:p.Ile52Ser
NM_001291969.1:c.118+4199T>G (POLH) NP_001278898.1:n.118+4199T>G
NM_001291970.1:c.341T>G (POLH) NP_001278899.1:p.Ile114Ser
NM_006502.2:c.341T>G , LRG_470t1:c.341T>G (POLH) NP_006493.1:p.Ile114Ser
XM_005249186.2:c.155T>G (POLH) XP_005249243.1:p.Ile52Ser
XM_011514698.1:c.118+4199T>G (POLH) XP_011513000.1:n.118+4199T>G
XM_005249186.4:c.155T>G (POLH) XP_005249243.1:p.Ile52Ser
XM_011514698.3:c.118+4199T>G (POLH) XP_011513000.1:n.118+4199T>G
XM_024446466.1:c.89T>G (POLH) XP_024302234.1:p.Ile30Ser
XM_024446467.1:c.-279T>G (POLH) XP_024302235.1:n.-279T>G
NM_001291969.2:c.118+4199T>G (POLH) NP_001278898.1:n.118+4199T>G
NM_001291970.2:c.341T>G (POLH) NP_001278899.1:p.Ile114Ser
NM_006502.3:c.341T>G (POLH) MANE Select NP_006493.1:p.Ile114Ser
NM_001318876.2:c.945+58069T>G (POLR1C) NP_001305805.1:n.945+58069T>G