Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153726096G>T , CM000685.2:g.153726096G>T | GRCh38 |
| NC_000023.10:g.152991551G>T , CM000685.1:g.152991551G>T | GRCh37 |
| NC_000023.9:g.152644745G>T | NCBI36 |
| NG_009022.2:g.6229G>T | |
| NG_023231.1:g.3651C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.830G>T MANE Select | NP_000024.2:p.Gly277Val |
| ENST00000218104.6:c.830G>T MANE Select | ENSP00000218104.3:p.Gly277Val |
| NM_000033.3:c.830G>T | NP_000024.2:p.Gly277Val |
| ENST00000218104.5:c.830G>T | ENSP00000218104.3:p.Gly277Val |
| ENST00000370129.4:c.275G>T | ENSP00000359147.3:p.Gly92Val |
| XR_938507.1:n.1246G>T | |
| XR_938507.2:n.1246G>T |