Linked Data
ClinVar Variation Id:
12702
ClinVar RCV Id:
RCV000013539
dbSNP Id:
rs137854433
PubMed:
PMID:16720658
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.132898809T>C , CM000670.2:g.132898809T>C | GRCh38 |
| NC_000008.10:g.133911054T>C , CM000670.1:g.133911054T>C | GRCh37 |
| NC_000008.9:g.133980236T>C | NCBI36 |
| NG_015832.1:g.36850T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000220616.9:c.3229T>C MANE Select | ENSP00000220616.4:p.Cys1077Arg | |
| ENST00000220616.8:c.3229T>C | ENSP00000220616.4:p.Cys1077Arg | |
| ENST00000518097.1:n.143T>C | ||
| ENST00000518505.1:c.129T>C | ||
| ENST00000523756.5:c.188T>C | ||
| NM_003235.4:c.3229T>C | NP_003226.4:p.Cys1077Arg | |
| XM_005251038.3:c.3229T>C | XP_005251095.1:p.Cys1077Arg | |
| XM_005251040.3:c.3229T>C | XP_005251097.1:p.Cys1077Arg | |
| XM_005251042.3:c.3229T>C | XP_005251099.1:p.Cys1077Arg | |
| XM_005251043.3:c.3229T>C | XP_005251100.1:p.Cys1077Arg | |
| XM_006716622.2:c.3229T>C | XP_006716685.1:p.Cys1077Arg | |
| XM_005251038.4:c.3229T>C | XP_005251095.1:p.Cys1077Arg | |
| XM_005251040.4:c.3229T>C | XP_005251097.1:p.Cys1077Arg | |
| XM_005251042.4:c.3229T>C | XP_005251099.1:p.Cys1077Arg | |
| XM_006716622.3:c.3229T>C | XP_006716685.1:p.Cys1077Arg | |
| XM_017013793.1:c.3229T>C | XP_016869282.1:p.Cys1077Arg | |
| XM_017013794.1:c.3229T>C | XP_016869283.1:p.Cys1077Arg | |
| XM_017013795.1:c.3229T>C | XP_016869284.1:p.Cys1077Arg | |
| XM_017013796.1:c.3229T>C | XP_016869285.1:p.Cys1077Arg | |
| XM_017013797.1:c.2968T>C | XP_016869286.1:p.Cys990Arg | |
| XM_017013798.1:c.3229T>C | XP_016869287.1:p.Cys1077Arg | |
| XM_017013799.1:c.3229T>C | XP_016869288.1:p.Cys1077Arg | |
| XM_017013800.1:c.3229T>C | XP_016869289.1:p.Cys1077Arg | |
| NM_003235.5:c.3229T>C MANE Select | NP_003226.4:p.Cys1077Arg |