Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48410637C= , CM000677.2:g.48410637C= | GRCh38 |
| NC_000015.9:g.48702834C= , CM000677.1:g.48702834C= | GRCh37 |
| NC_000015.8:g.46490126C= | NCBI36 |
| NG_008805.2:g.240152G= , LRG_778:g.240152G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*1777G= | ENSP00000453958.2:n.*1777G= | |
| ENST00000682158.1:n.2350G= | ||
| ENST00000682170.1:n.3150G= | ||
| ENST00000682767.1:n.2266G= | ||
| ENST00000316623.10:c.*353G= MANE Select | ENSP00000325527.5:n.*353G= | |
| ENST00000316623.9:c.*353G= | ENSP00000325527.5:n.*353G= | |
| ENST00000559133.5:c.4338G= | ||
| NM_000138.4:c.*353G= , LRG_778t1:c.*353G= | NP_000129.3:n.*353G= | |
| NM_000138.5:c.*353G= MANE Select | NP_000129.3:n.*353G= |