Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86575866G= , CM000670.2:g.86575866G= | GRCh38 |
| NC_000008.10:g.87588094G= , CM000670.1:g.87588094G= | GRCh37 |
| NC_000008.9:g.87657210G= | NCBI36 |
| NG_016980.1:g.172810C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.2368C= MANE Select | ENSP00000316605.5:p.Pro790= | |
| ENST00000681546.1:n.2188C= | ||
| ENST00000681746.1:c.*779C= | ENSP00000505959.1:n.*779C= | |
| ENST00000320005.5:c.2368C= | ENSP00000316605.5:p.Pro790= | |
| ENST00000517327.5:c.276+2823C= | ENSP00000428329.1:n.276+2823C= | |
| NM_019098.4:c.2368C= | NP_061971.3:p.Pro790= | |
| XM_011517138.1:c.1954C= | XP_011515440.1:p.Pro652= | |
| XM_011517138.2:c.1954C= | XP_011515440.1:p.Pro652= | |
| NM_019098.5:c.2368C= MANE Select | NP_061971.3:p.Pro790= |