Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74338761A>C , CM000677.2:g.74338761A>C | GRCh38 |
| NC_000015.9:g.74631102A>C , CM000677.1:g.74631102A>C | GRCh37 |
| NC_000015.8:g.72418155A>C | NCBI36 |
| NG_007973.1:g.33981T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000781.3:c.1244T>G MANE Select | NP_000772.2:p.Val415Gly |
| ENST00000268053.11:c.1244T>G MANE Select | ENSP00000268053.6:p.Val415Gly |
| NM_000781.2:c.1244T>G | NP_000772.2:p.Val415Gly |
| NM_001099773.1:c.770T>G | NP_001093243.1:p.Val257Gly |
| NM_001099773.2:c.770T>G | NP_001093243.1:p.Val257Gly |
| ENST00000268053.10:c.1244T>G | ENSP00000268053.6:p.Val415Gly |
| ENST00000358632.8:c.770T>G | ENSP00000351455.4:p.Val257Gly |
| ENST00000435365.5:c.1165T>G | ENSP00000391081.1:p.Cys389Gly |
| ENST00000498141.1:n.87T>G |