Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18786145C>A , CM000681.2:g.18786145C>A | GRCh38 |
| NC_000019.9:g.18896955C>A , CM000681.1:g.18896955C>A | GRCh37 |
| NC_000019.8:g.18757955C>A | NCBI36 |
| NG_007070.1:g.10160G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1309G>T MANE Select | ENSP00000222271.2:p.Asp437Tyr | |
| ENST00000222271.6:c.1309G>T | ENSP00000222271.2:p.Asp437Tyr | |
| ENST00000425807.1:c.1150G>T | ENSP00000403792.1:p.Asp384Tyr | |
| ENST00000542601.6:c.1210G>T | ENSP00000439156.2:p.Asp404Tyr | |
| ENST00000612179.1:n.559G>T | ||
| NM_000095.2:c.1309G>T | NP_000086.2:p.Asp437Tyr | |
| NM_000095.3:c.1309G>T MANE Select | NP_000086.2:p.Asp437Tyr |