Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115531C= , CM000681.2:g.10115531C= | GRCh38 |
| NC_000019.9:g.10226207C= , CM000681.1:g.10226207C= | GRCh37 |
| NC_000019.8:g.10087207C= | NCBI36 |
| NG_047007.1:g.9011C= | |
| NG_051197.1:g.9394G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.895G= MANE Select | ENSP00000253108.3:p.Gly299= | |
| ENST00000253108.8:c.895G= | ENSP00000253108.3:p.Gly299= | |
| ENST00000590158.1:n.914G= | ||
| ENST00000593054.5:c.289G= | ENSP00000467187.1:p.Gly97= | |
| NM_003755.3:c.895G= | NP_003746.2:p.Gly299= | |
| NM_003755.4:c.895G= | NP_003746.2:p.Gly299= | |
| NM_003755.5:c.895G= MANE Select | NP_003746.2:p.Gly299= |