Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.83509019T>C , CM000685.2:g.83509019T>C | GRCh38 |
| NC_000023.10:g.82764027T>C , CM000685.1:g.82764027T>C | GRCh37 |
| NC_000023.9:g.82650683T>C | NCBI36 |
| NG_009936.2:g.5759T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000307.5:c.695T>C MANE Select | NP_000298.3:p.Ile232Thr |
| ENST00000644024.2:c.695T>C MANE Select | ENSP00000495996.1:p.Ile232Thr |
| NM_000307.4:c.695T>C | NP_000298.3:p.Ile232Thr |
| ENST00000373200.4:c.695T>C | ENSP00000362296.2:p.Ile232Thr |