Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48974630T= , CM000681.2:g.48974630T= | GRCh38 |
| NC_000019.9:g.49477887T= , CM000681.1:g.49477887T= | GRCh37 |
| NC_000019.8:g.54169699T= | NCBI36 |
| NG_012923.1:g.23724A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323798.8:c.1412A= MANE Select | ENSP00000317904.3:p.Asp471= | |
| ENST00000263276.6:c.1220A= | ENSP00000263276.6:p.Asp407= | |
| ENST00000323798.7:c.1412A= | ENSP00000317904.3:p.Asp471= | |
| ENST00000472004.5:n.167A= | ||
| ENST00000496048.1:n.319A= | ||
| NM_001161587.1:c.1220A= | NP_001155059.1:p.Asp407= | |
| NM_002103.4:c.1412A= | NP_002094.2:p.Asp471= | |
| NR_027763.1:n.1471A= | ||
| NM_002103.5:c.1412A= MANE Select | NP_002094.2:p.Asp471= | |
| NM_001161587.2:c.1220A= | NP_001155059.1:p.Asp407= | |
| NR_027763.2:n.1427A= |