HGVS | Genome Assembly |
---|---|
NC_000001.11:g.28834651A>G , CM000663.2:g.28834651A>G | GRCh38 |
NC_000001.10:g.29161163A>G , CM000663.1:g.29161163A>G | GRCh37 |
NC_000001.9:g.29033750A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000234961.7:c.227+22041A>G MANE Select | ENSP00000234961.2:n.227+22041A>G | |
ENST00000234961.6:c.227+22041A>G | ENSP00000234961.2:n.227+22041A>G | |
ENST00000621425.1:c.227+22041A>G | ENSP00000477970.1:n.227+22041A>G | |
NM_000911.3:c.227+22041A>G | NP_000902.3:n.227+22041A>G | |
NM_000911.4:c.227+22041A>G MANE Select | NP_000902.3:n.227+22041A>G |