Canonical Allele Identifier: CA450293280

Linked Data

gnomAD v4: 6-43587455-A-G
MyVariant Identifiers: chr6:g.43555192A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43587455A>G , CM000668.2:g.43587455A>G GRCh38
NC_000006.11:g.43555192A>G , CM000668.1:g.43555192A>G GRCh37
NC_000006.10:g.43663170A>G NCBI36
NG_009252.1:g.16315A>G , LRG_470:g.16315A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372236.9:c.456A>G (POLH) MANE Select ENSP00000361310.4:p.Gln152=
ENST00000372226.1:c.456A>G (POLH) ENSP00000361300.1:p.Gln152=
ENST00000372236.8:c.456A>G (POLH) ENSP00000361310.4:p.Gln152=
NM_001291969.1:c.118+4314A>G (POLH) NP_001278898.1:n.118+4314A>G
NM_001291970.1:c.456A>G (POLH) NP_001278899.1:p.Gln152=
NM_006502.2:c.456A>G , LRG_470t1:c.456A>G (POLH) NP_006493.1:p.Gln152=
XM_005249186.2:c.270A>G (POLH) XP_005249243.1:p.Gln90=
XM_011514698.1:c.118+4314A>G (POLH) XP_011513000.1:n.118+4314A>G
XM_005249186.4:c.270A>G (POLH) XP_005249243.1:p.Gln90=
XM_011514698.3:c.118+4314A>G (POLH) XP_011513000.1:n.118+4314A>G
XM_024446466.1:c.204A>G (POLH) XP_024302234.1:p.Gln68=
XM_024446467.1:c.-164A>G (POLH) XP_024302235.1:n.-164A>G
NM_001291969.2:c.118+4314A>G (POLH) NP_001278898.1:n.118+4314A>G
NM_001291970.2:c.456A>G (POLH) NP_001278899.1:p.Gln152=
NM_006502.3:c.456A>G (POLH) MANE Select NP_006493.1:p.Gln152=
NM_001318876.2:c.945+58184A>G (POLR1C) NP_001305805.1:n.945+58184A>G