HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67585231A>T , CM000673.2:g.67585231A>T | GRCh38 |
NC_000011.9:g.67352702A>T , CM000673.1:g.67352702A>T | GRCh37 |
NC_000011.8:g.67109278A>T | NCBI36 |
NG_012075.1:g.6637A>T , LRG_723:g.6637A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000398603.6:c.326A>T | ENSP00000381604.1:p.Tyr109Phe | |
ENST00000398606.10:c.326A>T MANE Select | ENSP00000381607.3:p.Tyr109Phe | |
ENST00000646888.1:c.*42A>T | ENSP00000494477.1:n.*42A>T | |
ENST00000398603.5:c.326A>T | ENSP00000381604.1:p.Tyr109Phe | |
ENST00000398606.7:c.326A>T | ENSP00000381607.3:p.Tyr109Phe | |
ENST00000467591.1:n.437A>T | ||
ENST00000494593.1:n.1121A>T | ||
ENST00000498765.5:c.389A>T | ||
NM_000852.3:c.326A>T , LRG_723t1:c.326A>T | NP_000843.1:p.Tyr109Phe | |
NM_000852.4:c.326A>T MANE Select | NP_000843.1:p.Tyr109Phe |