Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94062642C= , CM000663.2:g.94062642C= | GRCh38 |
| NC_000001.10:g.94528198C= , CM000663.1:g.94528198C= | GRCh37 |
| NC_000001.9:g.94300786C= | NCBI36 |
| NG_009073.1:g.63508G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.1872G= MANE Select | ENSP00000359245.3:p.Val624= | |
| ENST00000649773.1:c.1872G= | ENSP00000496882.1:p.Val624= | |
| ENST00000370225.3:c.1872G= | ENSP00000359245.3:p.Val624= | |
| ENST00000536513.5:c.-65+532G= | ENSP00000439707.2:n.-65+532G= | |
| NM_000350.2:c.1872G= | NP_000341.2:p.Val624= | |
| NM_000350.3:c.1872G= MANE Select | NP_000341.2:p.Val624= |