Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94063218C= , CM000663.2:g.94063218C= | GRCh38 |
| NC_000001.10:g.94528774C= , CM000663.1:g.94528774C= | GRCh37 |
| NC_000001.9:g.94301362C= | NCBI36 |
| NG_009073.1:g.62932G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.1654G= MANE Select | NP_000341.2:p.Val552= |
| ENST00000370225.4:c.1654G= MANE Select | ENSP00000359245.3:p.Val552= |
| NM_000350.2:c.1654G= | NP_000341.2:p.Val552= |
| ENST00000370225.3:c.1654G= | ENSP00000359245.3:p.Val552= |
| ENST00000536513.5:c.-109G= | ENSP00000439707.2:n.-109G= |
| ENST00000649773.1:c.1654G= | ENSP00000496882.1:p.Val552= |