Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226753C= , CM000673.2:g.5226753C= | GRCh38 |
| NC_000011.9:g.5247983C= , CM000673.1:g.5247983C= | GRCh37 |
| NC_000011.8:g.5204559C= | NCBI36 |
| NG_000007.3:g.70863G= | |
| NG_059281.1:g.5319G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000518.5:c.139G= MANE Select | NP_000509.1:p.Gly47= |
| ENST00000335295.4:c.139G= MANE Select | ENSP00000333994.3:p.Gly47= |
| NM_000518.4:c.139G= | NP_000509.1:p.Gly47= |
| ENST00000380315.2:c.139G= | ENSP00000369671.2:p.Gly47= |
| ENST00000475226.1:n.71G= | |
| ENST00000485743.1:n.190G= | |
| ENST00000633227.1:c.123G= | ENSP00000488004.1:p.Leu41= |
| ENST00000647020.1:c.139G= | ENSP00000494175.1:p.Gly47= |