HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312711T>A , CM000673.2:g.118312711T>A | GRCh38 |
NC_000011.9:g.118183426T>A , CM000673.1:g.118183426T>A | GRCh37 |
NC_000011.8:g.117688636T>A | NCBI36 |
NG_007383.1:g.13132T>A , LRG_38:g.13132T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.197T>A MANE Select | ENSP00000354566.4:p.Ile66Lys | |
ENST00000361763.8:c.197T>A | ENSP00000354566.4:p.Ile66Lys | |
ENST00000526146.5:n.743T>A | ||
ENST00000528435.5:n.750T>A | ||
ENST00000528600.1:c.179T>A | ENSP00000433975.1:p.Ile60Lys | |
ENST00000529713.5:n.303T>A | ||
ENST00000531913.1:n.568T>A | ||
NM_000733.3:c.197T>A , LRG_38t1:c.197T>A | NP_000724.1:p.Ile66Lys | |
NM_000733.4:c.197T>A MANE Select | NP_000724.1:p.Ile66Lys |