Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8073213C>A , CM000679.2:g.8073213C>A | GRCh38 |
| NC_000017.10:g.7976531C>A , CM000679.1:g.7976531C>A | GRCh37 |
| NC_000017.9:g.7917256C>A | NCBI36 |
| NG_007099.1:g.19491G>T | |
| NG_007099.2:g.19504G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001139.3:c.1861G>T MANE Select | NP_001130.1:p.Asp621Tyr |
| ENST00000647874.1:c.1861G>T MANE Select | ENSP00000497784.1:p.Asp621Tyr |
| NM_001139.2:c.1861G>T | NP_001130.1:p.Asp621Tyr |
| ENST00000319144.4:c.1861G>T | ENSP00000315167.4:p.Asp621Tyr |
| ENST00000577351.5:n.585G>T | |
| ENST00000649809.1:c.925G>T | ENSP00000496845.1:p.Asp309Tyr |
| ENST00000650441.1:n.284G>T |