Linked Data
ClinVar Variation Id:
41210
dbSNP Id:
rs267606579
gnomAD v2:
11-67258282-C-T
gnomAD v4:
11-67490811-C-T
PubMed:
PMID:22720333
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67490811C>T , CM000673.2:g.67490811C>T | GRCh38 |
| NC_000011.9:g.67258282C>T , CM000673.1:g.67258282C>T | GRCh37 |
| NC_000011.8:g.67014858C>T | NCBI36 |
| NG_008969.1:g.12778C>T , LRG_460:g.12778C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525341.2:c.1118C>T | ||
| ENST00000528641.7:c.622C>T | ENSP00000434982.3:p.Arg208Trp | |
| ENST00000529797.2:n.1653C>T | ||
| ENST00000682324.1:c.469-186C>T | ENSP00000508017.1:n.469-186C>T | |
| ENST00000682659.1:c.442C>T | ENSP00000507351.1:p.Arg148Trp | |
| ENST00000682699.1:c.811C>T | ENSP00000507935.1:p.Arg271Trp | |
| ENST00000683237.1:c.803C>T | ENSP00000507343.1:p.Ala268Val | |
| ENST00000683856.1:c.634C>T | ENSP00000507979.1:p.Arg212Trp | |
| ENST00000684006.1:c.800C>T | ENSP00000507269.1:p.Ala267Val | |
| ENST00000684657.1:c.631C>T | ENSP00000507961.1:p.Arg211Trp | |
| ENST00000279146.8:c.811C>T MANE Select | ENSP00000279146.3:p.Arg271Trp | |
| ENST00000279146.7:c.811C>T | ENSP00000279146.3:p.Arg271Trp | |
| ENST00000528641.6:c.622C>T | ENSP00000434982.2:p.Arg208Trp | |
| NM_001302959.1:c.634C>T | NP_001289888.1:p.Arg212Trp | |
| NM_001302960.1:c.803C>T | NP_001289889.1:p.Ala268Val | |
| NM_003977.3:c.811C>T | NP_003968.3:p.Arg271Trp | |
| XM_024448761.1:c.811C>T | XP_024304529.1:p.Arg271Trp | |
| NM_003977.4:c.811C>T MANE Select | NP_003968.3:p.Arg271Trp | |
| NM_001302960.2:c.803C>T | NP_001289889.1:p.Ala268Val | |
| NM_001302959.2:c.634C>T | NP_001289888.1:p.Arg212Trp |