Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226577C= , CM000673.2:g.5226577C= | GRCh38 |
| NC_000011.9:g.5247807C= , CM000673.1:g.5247807C= | GRCh37 |
| NC_000011.8:g.5204383C= | NCBI36 |
| NG_000007.3:g.71039G= | |
| NG_059281.1:g.5495G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647020.1:c.315G= | ENSP00000494175.1:p.Arg105= | |
| ENST00000335295.4:c.315G= MANE Select | ENSP00000333994.3:p.Arg105= | |
| ENST00000475226.1:n.247G= | ||
| ENST00000485743.1:n.366G= | ||
| ENST00000633227.1:c.*131G= | ENSP00000488004.1:n.*131G= | |
| NM_000518.4:c.315G= | NP_000509.1:p.Arg105= | |
| NM_000518.5:c.315G= MANE Select | NP_000509.1:p.Arg105= |