HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586544G>T , CM000673.2:g.67586544G>T | GRCh38 |
NC_000011.9:g.67354015G>T , CM000673.1:g.67354015G>T | GRCh37 |
NC_000011.8:g.67110591G>T | NCBI36 |
NG_012075.1:g.7950G>T , LRG_723:g.7950G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.492G>T | ENSP00000381604.1:p.Val164= | |
ENST00000398606.10:c.600G>T MANE Select | ENSP00000381607.3:p.Val200= | |
ENST00000398603.5:c.492G>T | ENSP00000381604.1:p.Val164= | |
ENST00000398606.7:c.600G>T | ENSP00000381607.3:p.Val200= | |
ENST00000467591.1:n.711G>T | ||
ENST00000494593.1:n.1572G>T | ||
ENST00000498765.5:c.663G>T | ||
NM_000852.3:c.600G>T , LRG_723t1:c.600G>T | NP_000843.1:p.Val200= | |
NM_000852.4:c.600G>T MANE Select | NP_000843.1:p.Val200= |