Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115738247A>G , CM000663.2:g.115738247A>G | GRCh38 |
| NC_000001.10:g.116280868A>G , CM000663.1:g.116280868A>G | GRCh37 |
| NC_000001.9:g.116082391A>G | NCBI36 |
| NG_008802.1:g.35559T>C , LRG_404:g.35559T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000488931.2:c.233T>C | ENSP00000518226.1:p.Phe78Ser | |
| ENST00000261448.6:c.509T>C MANE Select | ENSP00000261448.5:p.Phe170Ser | |
| ENST00000261448.5:c.509T>C | ENSP00000261448.5:p.Phe170Ser | |
| NM_001232.3:c.509T>C , LRG_404t1:c.509T>C | NP_001223.2:p.Phe170Ser | |
| NM_001232.4:c.509T>C MANE Select | NP_001223.2:p.Phe170Ser |