Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189564068A= , CM000664.2:g.189564068A= | GRCh38 |
| NC_000002.11:g.190428794A= , CM000664.1:g.190428794A= | GRCh37 |
| NC_000002.10:g.190137039A= | NCBI36 |
| NG_009027.1:g.21744T= , LRG_837:g.21744T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261024.7:c.918T= MANE Select | ENSP00000261024.3:p.Pro306= | |
| ENST00000261024.6:c.918T= | ENSP00000261024.2:p.Pro306= | |
| NM_014585.5:c.918T= , LRG_837t1:c.918T= | NP_055400.1:p.Pro306= | |
| XM_005246505.1:c.798T= | XP_005246562.1:p.Pro266= | |
| XM_005246505.2:c.798T= | XP_005246562.1:p.Pro266= | |
| XM_017003938.2:c.798T= | XP_016859427.1:p.Pro266= | |
| NM_014585.6:c.918T= MANE Select | NP_055400.1:p.Pro306= |