Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133373269G= , CM000672.2:g.133373269G= | GRCh38 |
| NC_000010.10:g.135186773G= , CM000672.1:g.135186773G= | GRCh37 |
| NC_000010.9:g.135036763G= | NCBI36 |
| NG_042077.1:g.5136C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368547.4:c.65C= MANE Select | ENSP00000357535.3:p.Pro22= | |
| ENST00000368547.3:c.65C= | ENSP00000357535.3:p.Pro22= | |
| NM_004092.3:c.65C= | NP_004083.3:p.Pro22= | |
| XR_002956965.1:n.128C= | ||
| NM_004092.4:c.65C= MANE Select | NP_004083.3:p.Pro22= |