Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18785969C= , CM000681.2:g.18785969C= | GRCh38 |
| NC_000019.9:g.18896779C= , CM000681.1:g.18896779C= | GRCh37 |
| NC_000019.8:g.18757779C= | NCBI36 |
| NG_007070.1:g.10336G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1485G= MANE Select | ENSP00000222271.2:p.Ala495= | |
| ENST00000222271.6:c.1485G= | ENSP00000222271.2:p.Ala495= | |
| ENST00000425807.1:c.1326G= | ENSP00000403792.1:p.Ala442= | |
| ENST00000542601.6:c.1386G= | ENSP00000439156.2:p.Ala462= | |
| NM_000095.2:c.1485G= | NP_000086.2:p.Ala495= | |
| NM_000095.3:c.1485G= MANE Select | NP_000086.2:p.Ala495= |