Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046338T>G , CM000667.2:g.136046338T>G | GRCh38 |
| NC_000005.9:g.135382027T>G , CM000667.1:g.135382027T>G | GRCh37 |
| NC_000005.8:g.135409926T>G | NCBI36 |
| NG_012646.1:g.22444T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.302T>G MANE Select | ENSP00000416330.2:p.Leu101Arg | |
| ENST00000442011.6:c.302T>G | ENSP00000416330.2:p.Leu101Arg | |
| ENST00000504185.5:n.459T>G | ||
| ENST00000506699.5:n.367T>G | ||
| ENST00000507018.5:c.219T>G | ||
| ENST00000515433.1:n.594T>G | ||
| NM_000358.2:c.302T>G | NP_000349.1:p.Leu101Arg | |
| NM_000358.3:c.302T>G MANE Select | NP_000349.1:p.Leu101Arg |