Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119320748G= , CM000666.2:g.119320748G= | GRCh38 |
| NC_000004.11:g.120241903G= , CM000666.1:g.120241903G= | GRCh37 |
| NC_000004.10:g.120461351G= | NCBI36 |
| NG_011444.1:g.6414C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000274024.4:c.162C= MANE Select | ENSP00000274024.3:p.Ser54= | |
| ENST00000274024.3:c.162C= | ENSP00000274024.3:p.Ser54= | |
| NM_000134.3:c.162C= | NP_000125.2:p.Ser54= | |
| NM_000134.4:c.162C= MANE Select | NP_000125.2:p.Ser54= |