HGVS | Genome Assembly |
---|---|
NC_000015.10:g.78534647T= , CM000677.2:g.78534647T= | GRCh38 |
NC_000015.9:g.78826989T= , CM000677.1:g.78826989T= | GRCh37 |
NC_000015.8:g.76614044T= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000388988.9:c.*977T= MANE Select | ENSP00000373640.4:n.*977T= | |
ENST00000408962.6:c.662-2653T= | ENSP00000386197.2:n.662-2653T= | |
ENST00000563233.2:c.662-2653T= | ENSP00000454850.1:n.662-2653T= | |
ENST00000569878.5:c.2099T= | ENSP00000455459.1:n.2099T= | |
NM_001083612.1:c.662-2653T= | NP_001077081.1:n.662-2653T= | |
NM_001013619.3:c.*977T= | NP_001013641.2:n.*977T= | |
NM_001013619.4:c.*977T= MANE Select | NP_001013641.2:n.*977T= | |
NM_001083612.2:c.662-2653T= | NP_001077081.1:n.662-2653T= |