Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31326599A= , CM000680.2:g.31326599A= | GRCh38 |
| NC_000018.9:g.28906562A= , CM000680.1:g.28906562A= | GRCh37 |
| NC_000018.8:g.27160560A= | NCBI36 |
| NG_011803.2:g.13511A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000257192.5:c.67A= MANE Select | ENSP00000257192.4:p.Ser23= | |
| ENST00000257192.4:c.67A= | ENSP00000257192.4:p.Ser23= | |
| NM_001942.3:c.67A= | NP_001933.2:p.Ser23= | |
| NM_001942.4:c.67A= MANE Select | NP_001933.2:p.Ser23= |