Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.79916855G>A , CM000668.2:g.79916855G>A | GRCh38 |
| NC_000006.11:g.80626572G>A , CM000668.1:g.80626572G>A | GRCh37 |
| NC_000006.10:g.80683291G>A | NCBI36 |
| NG_009108.1:g.35744C>T | |
| NG_009108.2:g.35744C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022726.4:c.698C>T MANE Select | NP_073563.1:p.Thr233Met |
| ENST00000369816.5:c.698C>T MANE Select | ENSP00000358831.4:p.Thr233Met |
| NM_022726.3:c.698C>T | NP_073563.1:p.Thr233Met |
| ENST00000369816.4:c.698C>T | ENSP00000358831.4:p.Thr233Met |