Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99845631T>G , CM000672.2:g.99845631T>G | GRCh38 |
| NC_000010.10:g.101605388T>G , CM000672.1:g.101605388T>G | GRCh37 |
| NC_000010.9:g.101595378T>G | NCBI36 |
| NG_011798.1:g.67926T>G | |
| NG_011798.2:g.68034T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647814.1:c.3995T>G MANE Select | ENSP00000497274.1:p.Val1332Gly | |
| ENST00000649459.1:n.343T>G | ||
| ENST00000370449.8:c.3995T>G | ENSP00000359478.4:p.Val1332Gly | |
| NM_000392.4:c.3995T>G | NP_000383.1:p.Val1332Gly | |
| XM_006717630.2:c.3299T>G | XP_006717693.1:p.Val1100Gly | |
| XR_945604.1:n.4177-52T>G | ||
| XR_945605.1:n.4059T>G | ||
| NM_000392.5:c.3995T>G MANE Select | NP_000383.2:p.Val1332Gly | |
| XM_006717630.3:c.3299T>G | XP_006717693.1:p.Val1100Gly | |
| XR_945604.3:n.4231-52T>G | ||
| XR_945605.3:n.4111T>G |