HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67584706T>A , CM000673.2:g.67584706T>A | GRCh38 |
NC_000011.9:g.67352177T>A , CM000673.1:g.67352177T>A | GRCh37 |
NC_000011.8:g.67108753T>A | NCBI36 |
NG_012075.1:g.6112T>A , LRG_723:g.6112T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.166T>A | ENSP00000381604.1:p.Phe56Ile | |
ENST00000398606.10:c.166T>A MANE Select | ENSP00000381607.3:p.Phe56Ile | |
ENST00000646888.1:c.59T>A | ENSP00000494477.1:p.Val20Asp | |
ENST00000398603.5:c.166T>A | ENSP00000381604.1:p.Phe56Ile | |
ENST00000398606.7:c.166T>A | ENSP00000381607.3:p.Phe56Ile | |
ENST00000489040.1:n.165T>A | ||
ENST00000494593.1:n.596T>A | ||
ENST00000498765.5:c.129T>A | ||
NM_000852.3:c.166T>A , LRG_723t1:c.166T>A | NP_000843.1:p.Phe56Ile | |
NM_000852.4:c.166T>A MANE Select | NP_000843.1:p.Phe56Ile |