Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24290935A= , CM000668.2:g.24290935A= | GRCh38 |
| NC_000006.11:g.24291163A= , CM000668.1:g.24291163A= | GRCh37 |
| NC_000006.10:g.24399142A= | NCBI36 |
| NG_012829.1:g.72118T= | |
| NG_012829.2:g.97358T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_016356.5:c.701T= MANE Select | NP_057440.2:p.Phe234= |
| ENST00000378454.8:c.701T= MANE Select | ENSP00000367715.3:p.Phe234= |
| NM_001195610.1:c.701T= | NP_001182539.1:p.Phe234= |
| NM_001195610.2:c.701T= | NP_001182539.1:p.Phe234= |
| NM_016356.4:c.701T= | NP_057440.2:p.Phe234= |
| ENST00000378454.7:c.701T= | ENSP00000367715.3:p.Phe234= |