HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19951871C>A , CM000670.2:g.19951871C>A | GRCh38 |
NC_000008.10:g.19809382C>A , CM000670.1:g.19809382C>A | GRCh37 |
NC_000008.9:g.19853662C>A | NCBI36 |
NG_008855.1:g.17801C>A | |
NG_008855.2:g.55155C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.352C>A MANE Select | ENSP00000497642.1:p.Gln118Lys | |
ENST00000311322.8:c.352C>A | ENSP00000309757.6:p.Gln118Lys | |
ENST00000520959.5:c.124C>A | ENSP00000428496.1:p.Gln42Lys | |
ENST00000524029.5:c.352C>A | ENSP00000428237.1:p.Gln118Lys | |
NM_000237.2:c.352C>A | NP_000228.1:p.Gln118Lys | |
NM_000237.3:c.352C>A MANE Select | NP_000228.1:p.Gln118Lys |