HGVS | Genome Assembly |
---|---|
NC_000012.12:g.121627040G= , CM000674.2:g.121627040G= | GRCh38 |
NC_000012.11:g.122064946G= , CM000674.1:g.122064946G= | GRCh37 |
NC_000012.10:g.120549329G= | NCBI36 |
NG_007500.1:g.5466G= , LRG_93:g.5466G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698901.1:n.425+107G= | ||
ENST00000617316.2:c.293G= | ENSP00000482568.2:p.Gly98= | |
ENST00000646827.1:n.491G= | ||
ENST00000611718.1:c.104G= | ENSP00000477953.1:p.Gly35= | |
ENST00000616379.1:c.293G= | ENSP00000480616.1:p.Gly98= | |
ENST00000617316.1:c.104G= | ENSP00000482568.1:p.Gly35= | |
NM_032790.3:c.293G= , LRG_93t1:c.293G= | NP_116179.2:p.Gly98= |