Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.56594872T>G , CM000679.2:g.56594872T>G | GRCh38 |
| NC_000017.10:g.54672233T>G , CM000679.1:g.54672233T>G | GRCh37 |
| NC_000017.9:g.52027232T>G | NCBI36 |
| NG_011958.1:g.6174T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005450.6:c.649T>G MANE Select | NP_005441.1:p.Trp217Gly |
| ENST00000332822.6:c.649T>G MANE Select | ENSP00000328181.4:p.Trp217Gly |
| NM_005450.4:c.649T>G | NP_005441.1:p.Trp217Gly |
| ENST00000332822.4:c.649T>G | ENSP00000328181.4:p.Trp217Gly |