Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133373237C= , CM000672.2:g.133373237C= | GRCh38 |
| NC_000010.10:g.135186741C= , CM000672.1:g.135186741C= | GRCh37 |
| NC_000010.9:g.135036731C= | NCBI36 |
| NG_042077.1:g.5168G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368547.4:c.88+9G= MANE Select | ENSP00000357535.3:n.88+9G= | |
| ENST00000368547.3:c.88+9G= | ENSP00000357535.3:n.88+9G= | |
| NM_004092.3:c.88+9G= | NP_004083.3:n.88+9G= | |
| XR_002956965.1:n.151+9G= | ||
| NM_004092.4:c.88+9G= MANE Select | NP_004083.3:n.88+9G= |