Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24290935A>G , CM000668.2:g.24290935A>G | GRCh38 |
| NC_000006.11:g.24291163A>G , CM000668.1:g.24291163A>G | GRCh37 |
| NC_000006.10:g.24399142A>G | NCBI36 |
| NG_012829.1:g.72118T>C | |
| NG_012829.2:g.97358T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_016356.5:c.701T>C MANE Select | NP_057440.2:p.Phe234Ser |
| ENST00000378454.8:c.701T>C MANE Select | ENSP00000367715.3:p.Phe234Ser |
| NM_001195610.1:c.701T>C | NP_001182539.1:p.Phe234Ser |
| NM_001195610.2:c.701T>C | NP_001182539.1:p.Phe234Ser |
| NM_016356.4:c.701T>C | NP_057440.2:p.Phe234Ser |
| ENST00000378454.7:c.701T>C | ENSP00000367715.3:p.Phe234Ser |