Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.77518085C= , CM000676.2:g.77518085C= | GRCh38 |
| NC_000014.8:g.77984428C= , CM000676.1:g.77984428C= | GRCh37 |
| NC_000014.7:g.77054181C= | NCBI36 |
| NG_028282.1:g.103683G= , LRG_371:g.103683G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686627.1:n.554G= | ||
| ENST00000687688.1:n.1285G= | ||
| ENST00000692906.1:n.1254G= | ||
| ENST00000216484.7:c.1522G= MANE Select | ENSP00000216484.2:p.Ala508= | |
| ENST00000216484.6:c.1522G= | ENSP00000216484.2:p.Ala508= | |
| ENST00000556607.1:c.350G= | ENSP00000451029.1:n.350G= | |
| NM_004863.3:c.1522G= , LRG_371t1:c.1522G= | NP_004854.1:p.Ala508= | |
| NM_004863.4:c.1522G= MANE Select | NP_004854.1:p.Ala508= |