Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6224712C>A , CM000668.2:g.6224712C>A | GRCh38 |
| NC_000006.11:g.6224945C>A , CM000668.1:g.6224945C>A | GRCh37 |
| NC_000006.10:g.6169944C>A | NCBI36 |
| NG_008107.1:g.100980G>T , LRG_549:g.100980G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.947G>T MANE Select | ENSP00000264870.3:p.Trp316Leu | |
| ENST00000264870.7:c.947G>T | ENSP00000264870.3:p.Trp316Leu | |
| ENST00000445223.1:c.97G>T | ||
| NM_000129.3:c.947G>T , LRG_549t1:c.947G>T | NP_000120.2:p.Trp316Leu | |
| XM_006715010.2:c.947G>T | XP_006715073.1:p.Trp316Leu | |
| XM_011514342.1:c.1109G>T | XP_011512644.1:p.Trp370Leu | |
| NM_000129.4:c.947G>T MANE Select | NP_000120.2:p.Trp316Leu |