Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153726095G>T , CM000685.2:g.153726095G>T | GRCh38 |
| NC_000023.10:g.152991550G>T , CM000685.1:g.152991550G>T | GRCh37 |
| NC_000023.9:g.152644744G>T | NCBI36 |
| NG_009022.2:g.6228G>T | |
| NG_023231.1:g.3652C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.829G>T MANE Select | NP_000024.2:p.Gly277Trp |
| ENST00000218104.6:c.829G>T MANE Select | ENSP00000218104.3:p.Gly277Trp |
| NM_000033.3:c.829G>T | NP_000024.2:p.Gly277Trp |
| ENST00000218104.5:c.829G>T | ENSP00000218104.3:p.Gly277Trp |
| ENST00000370129.4:c.274G>T | ENSP00000359147.3:p.Gly92Trp |
| XR_938507.1:n.1245G>T | |
| XR_938507.2:n.1245G>T |