Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.103458365G= , CM000672.2:g.103458365G= | GRCh38 |
| NC_000010.10:g.105218122G= , CM000672.1:g.105218122G= | GRCh37 |
| NC_000010.9:g.105208112G= | NCBI36 |
| NG_016855.1:g.5527C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329905.6:c.387C= MANE Select | ENSP00000329926.6:p.Phe129= | |
| ENST00000329905.5:c.387C= | ENSP00000329926.5:p.Phe129= | |
| NM_001001412.3:c.387C= | NP_001001412.3:p.Phe129= | |
| NM_001001412.4:c.387C= MANE Select | NP_001001412.3:p.Phe129= |