Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6107594G= , CM000682.2:g.6107594G= | GRCh38 |
| NC_000020.10:g.6088241G= , CM000682.1:g.6088241G= | GRCh37 |
| NC_000020.9:g.6036241G= | NCBI36 |
| NG_016213.1:g.20951C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017671.5:c.787C= MANE Select | NP_060141.3:p.Gln263= |
| ENST00000217289.9:c.787C= MANE Select | ENSP00000217289.4:p.Gln263= |
| NM_017671.4:c.787C= | NP_060141.3:p.Gln263= |
| ENST00000217289.8:c.787C= | ENSP00000217289.4:p.Gln263= |
| ENST00000536936.1:c.16C= | ENSP00000441063.1:p.Gln6= |
| ENST00000699095.1:c.787C= | ENSP00000514127.1:p.Gln263= |
| ENST00000699096.1:n.1249C= | |
| ENST00000699098.1:c.787C= | ENSP00000514312.1:p.Gln263= |
| XM_024451935.1:c.787C= | XP_024307703.1:p.Gln263= |