Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48427699C= , CM000677.2:g.48427699C= | GRCh38 |
| NC_000015.9:g.48719896C= , CM000677.1:g.48719896C= | GRCh37 |
| NC_000015.8:g.46507188C= | NCBI36 |
| NG_008805.2:g.223090G= , LRG_778:g.223090G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000138.5:c.7072G= MANE Select | NP_000129.3:p.Val2358= |
| ENST00000316623.10:c.7072G= MANE Select | ENSP00000325527.5:p.Val2358= |
| NM_000138.4:c.7072G= , LRG_778t1:c.7072G= | NP_000129.3:p.Val2358= |
| ENST00000316623.9:c.7072G= | ENSP00000325527.5:p.Val2358= |
| ENST00000559133.5:c.2441G= | |
| ENST00000559133.6:c.7134G= | ENSP00000453958.2:p.Pro2378= |
| ENST00000674301.1:c.2238G= | ENSP00000501333.1:n.2238G= |
| ENST00000674301.2:c.*585G= | ENSP00000501333.2:n.*585G= |
| ENST00000682170.1:n.1253G= | |
| ENST00000682767.1:n.369G= |