HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67585189A>T , CM000673.2:g.67585189A>T | GRCh38 |
NC_000011.9:g.67352660A>T , CM000673.1:g.67352660A>T | GRCh37 |
NC_000011.8:g.67109236A>T | NCBI36 |
NG_012075.1:g.6595A>T , LRG_723:g.6595A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.284A>T | ENSP00000381604.1:p.Asp95Val | |
ENST00000398606.10:c.284A>T MANE Select | ENSP00000381607.3:p.Asp95Val | |
ENST00000646888.1:c.177A>T | ENSP00000494477.1:p.Ter59Cys | |
ENST00000398603.5:c.284A>T | ENSP00000381604.1:p.Asp95Val | |
ENST00000398606.7:c.284A>T | ENSP00000381607.3:p.Asp95Val | |
ENST00000467591.1:n.395A>T | ||
ENST00000494593.1:n.1079A>T | ||
ENST00000498765.5:c.347A>T | ||
NM_000852.3:c.284A>T , LRG_723t1:c.284A>T | NP_000843.1:p.Asp95Val | |
NM_000852.4:c.284A>T MANE Select | NP_000843.1:p.Asp95Val |