Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226606T= , CM000673.2:g.5226606T= | GRCh38 |
| NC_000011.9:g.5247836T= , CM000673.1:g.5247836T= | GRCh37 |
| NC_000011.8:g.5204412T= | NCBI36 |
| NG_000007.3:g.71010A= | |
| NG_059281.1:g.5466A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000518.5:c.286A= MANE Select | NP_000509.1:p.Lys96= |
| ENST00000335295.4:c.286A= MANE Select | ENSP00000333994.3:p.Lys96= |
| NM_000518.4:c.286A= | NP_000509.1:p.Lys96= |
| ENST00000475226.1:n.218A= | |
| ENST00000485743.1:n.337A= | |
| ENST00000633227.1:c.*102A= | ENSP00000488004.1:n.*102A= |
| ENST00000647020.1:c.286A= | ENSP00000494175.1:p.Lys96= |