Linked Data
ClinVar Variation Id:
16129
dbSNP Id:
rs121909737
gnomAD v4:
10-87061009-C-T
PubMed:
PMID:11214910
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87061009C>T , CM000672.2:g.87061009C>T | GRCh38 |
| NC_000010.10:g.88820766C>T , CM000672.1:g.88820766C>T | GRCh37 |
| NC_000010.9:g.88810746C>T | NCBI36 |
| NG_013010.1:g.39011G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474574.2:n.2540G>A | ||
| ENST00000487058.2:n.177G>A | ||
| ENST00000681987.1:n.803G>A | ||
| ENST00000681988.1:c.464G>A | ENSP00000507316.1:p.Arg155His | |
| ENST00000682396.1:c.956G>A | ENSP00000506764.1:n.956G>A | |
| ENST00000682507.1:c.464G>A | ENSP00000508098.1:p.Arg155His | |
| ENST00000682622.1:c.1245G>A | ENSP00000506732.1:n.1245G>A | |
| ENST00000682833.1:c.800G>A | ||
| ENST00000683022.1:c.986G>A | ||
| ENST00000683256.1:c.464G>A | ENSP00000507901.1:p.Arg155His | |
| ENST00000683269.1:c.464G>A | ENSP00000508107.1:p.Arg155His | |
| ENST00000683647.1:n.4299G>A | ||
| ENST00000683783.1:c.464G>A | ENSP00000507881.1:p.Arg155His | |
| ENST00000683813.1:n.693G>A | ||
| ENST00000684032.1:c.820G>A | ENSP00000506969.1:n.820G>A | |
| ENST00000684201.1:c.922-768G>A | ENSP00000507887.1:n.922-768G>A | |
| ENST00000684338.1:c.965G>A | ENSP00000507457.1:p.Arg322His | |
| ENST00000684372.1:c.464G>A | ENSP00000508244.1:p.Arg155His | |
| ENST00000684392.1:n.1696G>A | ||
| ENST00000684434.1:c.436G>A | ||
| ENST00000684546.1:c.464G>A | ENSP00000507729.1:p.Arg155His | |
| ENST00000684690.1:n.746G>A | ||
| ENST00000684699.1:n.3098G>A | ||
| ENST00000277865.5:c.965G>A MANE Select | ENSP00000277865.4:p.Arg322His | |
| ENST00000277865.4:c.965G>A | ENSP00000277865.4:p.Arg322His | |
| ENST00000465164.1:n.44G>A | ||
| ENST00000474574.1:n.338G>A | ||
| NM_005271.3:c.965G>A | NP_005262.1:p.Arg322His | |
| XM_011539668.1:c.464G>A | XP_011537970.1:p.Arg155His | |
| XM_011539669.1:c.464G>A | XP_011537971.1:p.Arg155His | |
| NM_001318900.1:c.566G>A | NP_001305829.1:p.Arg189His | |
| NM_001318901.1:c.464G>A | NP_001305830.1:p.Arg155His | |
| NM_001318902.1:c.464G>A | NP_001305831.1:p.Arg155His | |
| NM_001318904.1:c.464G>A | NP_001305833.1:p.Arg155His | |
| NM_001318905.1:c.464G>A | NP_001305834.1:p.Arg155His | |
| NM_001318906.1:c.464G>A | NP_001305835.1:p.Arg155His | |
| NM_005271.4:c.965G>A | NP_005262.1:p.Arg322His | |
| NM_005271.5:c.965G>A MANE Select | NP_005262.1:p.Arg322His | |
| NM_001318904.2:c.464G>A | NP_001305833.1:p.Arg155His | |
| NM_001318905.2:c.464G>A | NP_001305834.1:p.Arg155His | |
| NM_001318906.2:c.464G>A | NP_001305835.1:p.Arg155His |