Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18400280T= , CM000670.2:g.18400280T= | GRCh38 |
| NC_000008.10:g.18257790T= , CM000670.1:g.18257790T= | GRCh37 |
| NC_000008.9:g.18302070T= | NCBI36 |
| NG_012246.1:g.14036T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286479.4:c.277T= MANE Select | ENSP00000286479.3:p.Phe93= | |
| ENST00000286479.3:c.277T= | ENSP00000286479.3:p.Phe93= | |
| ENST00000520116.1:c.-57-57T= | ENSP00000428416.1:n.-57-57T= | |
| NM_000015.2:c.277T= | NP_000006.2:p.Phe93= | |
| XM_011544358.1:c.277T= | XP_011542660.1:p.Phe93= | |
| XM_017012938.1:c.277T= | XP_016868427.1:p.Phe93= | |
| NM_000015.3:c.277T= MANE Select | NP_000006.2:p.Phe93= |