Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.76346249T= , CM000674.2:g.76346249T= | GRCh38 |
| NC_000012.11:g.76740029T= , CM000674.1:g.76740029T= | GRCh37 |
| NC_000012.10:g.75264160T= | NCBI36 |
| NG_016357.1:g.7194A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_024685.4:c.1736A= MANE Select | NP_078961.3:p.Lys579= |
| ENST00000650064.2:c.1736A= MANE Select | ENSP00000497413.1:p.Lys579= |
| NM_024685.3:c.1736A= | NP_078961.3:p.Lys579= |
| ENST00000393262.3:c.1736A= | ENSP00000376946.3:p.Lys579= |