Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136056794G= , CM000667.2:g.136056794G= | GRCh38 |
| NC_000005.9:g.135392483G= , CM000667.1:g.135392483G= | GRCh37 |
| NC_000005.8:g.135420382G= | NCBI36 |
| NG_012646.1:g.32900G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.1677G= MANE Select | ENSP00000416330.2:p.Leu559= | |
| ENST00000442011.6:c.1677G= | ENSP00000416330.2:p.Leu559= | |
| ENST00000506699.5:n.2194G= | ||
| ENST00000507018.5:c.1655G= | ||
| ENST00000509485.5:c.674G= | ||
| ENST00000514242.5:n.448G= | ||
| ENST00000514554.5:c.829G= | ||
| NM_000358.2:c.1677G= | NP_000349.1:p.Leu559= | |
| NM_000358.3:c.1677G= MANE Select | NP_000349.1:p.Leu559= |