Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.79916658T= , CM000668.2:g.79916658T= | GRCh38 |
| NC_000006.11:g.80626375T= , CM000668.1:g.80626375T= | GRCh37 |
| NC_000006.10:g.80683094T= | NCBI36 |
| NG_009108.1:g.35941A= | |
| NG_009108.2:g.35941A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022726.4:c.895A= MANE Select | NP_073563.1:p.Met299= |
| ENST00000369816.5:c.895A= MANE Select | ENSP00000358831.4:p.Met299= |
| NM_022726.3:c.895A= | NP_073563.1:p.Met299= |
| ENST00000369816.4:c.895A= | ENSP00000358831.4:p.Met299= |