Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47733732T>G , CM000679.2:g.47733732T>G | GRCh38 |
| NC_000017.10:g.45811098T>G , CM000679.1:g.45811098T>G | GRCh37 |
| NC_000017.9:g.43166097T>G | NCBI36 |
| NG_012166.1:g.5489T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000177694.2:c.278T>G MANE Select | ENSP00000177694.1:p.Phe93Cys | |
| ENST00000177694.1:c.278T>G | ENSP00000177694.1:p.Phe93Cys | |
| ENST00000581328.1:n.308T>G | ||
| NM_013351.1:c.278T>G | NP_037483.1:p.Phe93Cys | |
| XM_011524698.1:c.278T>G | XP_011523000.1:p.Phe93Cys | |
| NM_013351.2:c.278T>G MANE Select | NP_037483.1:p.Phe93Cys |