Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.77794569C>G , CM000671.2:g.77794569C>G | GRCh38 |
| NC_000009.11:g.80409485C>G , CM000671.1:g.80409485C>G | GRCh37 |
| NC_000009.10:g.79599305C>G | NCBI36 |
| NG_027904.2:g.241735G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286548.9:c.629G>C MANE Select | ENSP00000286548.4:p.Arg210Thr | |
| ENST00000286548.8:c.629G>C | ENSP00000286548.4:p.Arg210Thr | |
| NM_002072.4:c.629G>C | NP_002063.2:p.Arg210Thr | |
| XM_017014628.2:c.455G>C | XP_016870117.1:p.Arg152Thr | |
| NM_002072.5:c.629G>C MANE Select | NP_002063.2:p.Arg210Thr |