Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.30313780C= , CM000672.2:g.30313780C= | GRCh38 |
| NC_000010.10:g.30602709C= , CM000672.1:g.30602709C= | GRCh37 |
| NC_000010.9:g.30642715C= | NCBI36 |
| NG_028096.1:g.40559G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263063.9:c.1578G= MANE Select | ENSP00000263063.3:p.Gly526= | |
| ENST00000263063.8:c.1578G= | ENSP00000263063.3:p.Gly526= | |
| ENST00000488290.5:n.3333G= | ||
| NM_018109.3:c.1578G= | NP_060579.3:p.Gly526= | |
| NM_018109.4:c.1578G= MANE Select | NP_060579.3:p.Gly526= |