Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.59843896A>G , CM000673.2:g.59843896A>G | GRCh38 |
| NC_000011.9:g.59611369A>G , CM000673.1:g.59611369A>G | GRCh37 |
| NC_000011.8:g.59367945A>G | NCBI36 |
| NG_008120.1:g.6606T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000257248.3:c.239T>C MANE Select | ENSP00000257248.2:p.Met80Thr | |
| ENST00000257248.2:c.239T>C | ENSP00000257248.2:p.Met80Thr | |
| ENST00000525058.5:c.*206T>C | ENSP00000433196.1:n.*206T>C | |
| ENST00000532070.1:n.285T>C | ||
| NM_005142.2:c.239T>C | NP_005133.2:p.Met80Thr | |
| XM_011544939.1:c.239T>C | XP_011543241.1:p.Met80Thr | |
| XM_011544939.3:c.239T>C | XP_011543241.1:p.Met80Thr | |
| NM_005142.3:c.239T>C MANE Select | NP_005133.2:p.Met80Thr |