Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17024025G= , CM000663.2:g.17024025G= | GRCh38 |
| NC_000001.10:g.17350520G= , CM000663.1:g.17350520G= | GRCh37 |
| NC_000001.9:g.17223107G= | NCBI36 |
| NG_012340.1:g.35146C= , LRG_316:g.35146C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003000.3:c.590C= MANE Select | NP_002991.2:p.Pro197= |
| ENST00000375499.8:c.590C= MANE Select | ENSP00000364649.3:p.Pro197= |
| NM_003000.2:c.590C= , LRG_316t1:c.590C= | NP_002991.2:p.Pro197= |
| ENST00000375499.7:c.590C= | ENSP00000364649.3:p.Pro197= |
| ENST00000463045.3:c.419C= | ENSP00000481376.2:p.Pro140= |
| ENST00000485515.5:n.524C= | |
| ENST00000491274.5:c.548C= | ENSP00000480482.1:p.Pro183= |
| ENST00000491274.6:c.548C= | ENSP00000480482.2:p.Pro183= |