Linked Data
ClinVar Variation Id:
356902
dbSNP Id:
rs145530456
ExAC:
6:43568802 C / T
gnomAD v2:
6-43568802-C-T
gnomAD v3:
6-43601065-C-T
gnomAD v4:
6-43601065-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.43601065C>T , CM000668.2:g.43601065C>T | GRCh38 |
| NC_000006.11:g.43568802C>T , CM000668.1:g.43568802C>T | GRCh37 |
| NC_000006.10:g.43676780C>T | NCBI36 |
| NG_009252.1:g.29925C>T , LRG_470:g.29925C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372236.9:c.738C>T (POLH) MANE Select | ENSP00000361310.4:p.Leu246= | |
| ENST00000372226.1:c.738C>T (POLH) | ENSP00000361300.1:p.Leu246= | |
| ENST00000372236.8:c.738C>T (POLH) | ENSP00000361310.4:p.Leu246= | |
| NM_001291969.1:c.366C>T (POLH) | NP_001278898.1:p.Leu122= | |
| NM_001291970.1:c.738C>T (POLH) | NP_001278899.1:p.Leu246= | |
| NM_006502.2:c.738C>T , LRG_470t1:c.738C>T (POLH) | NP_006493.1:p.Leu246= | |
| XM_005249186.2:c.552C>T (POLH) | XP_005249243.1:p.Leu184= | |
| XM_011514698.1:c.366C>T (POLH) | XP_011513000.1:p.Leu122= | |
| XM_005249186.4:c.552C>T (POLH) | XP_005249243.1:p.Leu184= | |
| XM_011514698.3:c.366C>T (POLH) | XP_011513000.1:p.Leu122= | |
| XM_024446466.1:c.486C>T (POLH) | XP_024302234.1:p.Leu162= | |
| XM_024446467.1:c.282C>T (POLH) | XP_024302235.1:p.Leu94= | |
| NM_001291969.2:c.366C>T (POLH) | NP_001278898.1:p.Leu122= | |
| NM_001291970.2:c.738C>T (POLH) | NP_001278899.1:p.Leu246= | |
| NM_006502.3:c.738C>T (POLH) MANE Select | NP_006493.1:p.Leu246= | |
| NM_001318876.2:c.945+71794C>T (POLR1C) | NP_001305805.1:n.945+71794C>T |