Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29072487G>A , CM000664.2:g.29072487G>A | GRCh38 |
| NC_000002.11:g.29295353G>A , CM000664.1:g.29295353G>A | GRCh37 |
| NC_000002.10:g.29148857G>A | NCBI36 |
| NG_021427.1:g.6775C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001029883.3:c.1775C>T MANE Select | NP_001025054.1:p.Thr592Met |
| ENST00000331664.6:c.1775C>T MANE Select | ENSP00000332809.4:p.Thr592Met |
| NM_001029883.2:c.1775C>T | NP_001025054.1:p.Thr592Met |
| ENST00000331664.5:c.1775C>T | ENSP00000332809.4:p.Thr592Met |
| XM_011532826.1:c.1775C>T | XP_011531128.1:p.Thr592Met |
| XR_939901.1:n.185+3320G>A | |
| XR_939902.1:n.173+3332G>A |