Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6107547G>A , CM000682.2:g.6107547G>A | GRCh38 |
| NC_000020.10:g.6088194G>A , CM000682.1:g.6088194G>A | GRCh37 |
| NC_000020.9:g.6036194G>A | NCBI36 |
| NG_016213.1:g.20998C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699095.1:c.834C>T | ENSP00000514127.1:p.Phe278= | |
| ENST00000699096.1:n.1296C>T | ||
| ENST00000699097.1:n.4C>T | ||
| ENST00000699098.1:c.834C>T | ENSP00000514312.1:p.Phe278= | |
| ENST00000217289.9:c.834C>T MANE Select | ENSP00000217289.4:p.Phe278= | |
| ENST00000217289.8:c.834C>T | ENSP00000217289.4:p.Phe278= | |
| ENST00000536936.1:c.63C>T | ENSP00000441063.1:p.Phe21= | |
| NM_017671.4:c.834C>T | NP_060141.3:p.Phe278= | |
| XM_024451935.1:c.834C>T | XP_024307703.1:p.Phe278= | |
| NM_017671.5:c.834C>T MANE Select | NP_060141.3:p.Phe278= |