Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99221623T= , CM000671.2:g.99221623T= | GRCh38 |
| NC_000009.11:g.101983905T= , CM000671.1:g.101983905T= | GRCh37 |
| NC_000009.10:g.101023726T= | NCBI36 |
| NG_008928.1:g.5342A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476832.2:c.272A= MANE Select | ENSP00000417764.1:p.Tyr91= | |
| ENST00000238477.5:c.272A= | ENSP00000432675.2:p.Tyr91= | |
| ENST00000476832.1:c.272A= | ENSP00000417764.1:p.Tyr91= | |
| NM_033087.3:c.272A= | NP_149078.1:p.Tyr91= | |
| NR_024532.1:n.342A= | ||
| NM_033087.4:c.272A= MANE Select | NP_149078.1:p.Tyr91= | |
| NR_024532.2:n.320A= |