Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.26625603T= , CM000684.2:g.26625603T= | GRCh38 |
| NC_000022.10:g.27021567T= , CM000684.1:g.27021567T= | GRCh37 |
| NC_000022.9:g.25351567T= | NCBI36 |
| NG_009825.1:g.8640T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001886.3:c.281T= MANE Select | NP_001877.1:p.Phe94= |
| ENST00000354760.4:c.281T= MANE Select | ENSP00000346805.3:p.Phe94= |
| NM_001886.2:c.281T= | NP_001877.1:p.Phe94= |
| ENST00000354760.3:c.281T= | ENSP00000346805.3:p.Phe94= |
| ENST00000466315.1:n.178T= | |
| XM_006724140.2:c.296T= | XP_006724203.1:p.Phe99= |
| XM_006724140.3:c.296T= | XP_006724203.1:p.Phe99= |
| XM_011529898.1:c.395T= | XP_011528200.1:p.Phe132= |
| XM_017028598.1:c.314T= | XP_016884087.1:p.Phe105= |