Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.60371856C= , CM000680.2:g.60371856C= | GRCh38 |
| NC_000018.9:g.58039089C= , CM000680.1:g.58039089C= | GRCh37 |
| NC_000018.8:g.56190069C= | NCBI36 |
| NG_016441.1:g.5913G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005912.3:c.494G= MANE Select | NP_005903.2:p.Arg165= |
| ENST00000299766.5:c.494G= MANE Select | ENSP00000299766.3:p.Arg165= |
| NM_005912.2:c.494G= | NP_005903.2:p.Arg165= |
| ENST00000299766.4:c.494G= | ENSP00000299766.3:p.Arg165= |