Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5045669A= , CM000674.2:g.5045669A= | GRCh38 |
| NC_000012.11:g.5154835A= , CM000674.1:g.5154835A= | GRCh37 |
| NC_000012.10:g.5025096A= | NCBI36 |
| NG_012198.1:g.6751A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.1522A= MANE Select | ENSP00000252321.3:p.Ile508= | |
| ENST00000252321.4:c.1522A= | ENSP00000252321.3:p.Ile508= | |
| NM_002234.3:c.1522A= | NP_002225.2:p.Ile508= | |
| NM_002234.4:c.1522A= MANE Select | NP_002225.2:p.Ile508= |