HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19951786G= , CM000670.2:g.19951786G= | GRCh38 |
NC_000008.10:g.19809297G= , CM000670.1:g.19809297G= | GRCh37 |
NC_000008.9:g.19853577G= | NCBI36 |
NG_008855.1:g.17716G= | |
NG_008855.2:g.55070G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.267G= MANE Select | ENSP00000497642.1:p.Glu89= | |
ENST00000311322.8:c.267G= | ENSP00000309757.6:p.Glu89= | |
ENST00000520959.5:c.39G= | ENSP00000428496.1:p.Glu13= | |
ENST00000521994.1:n.524G= | ||
ENST00000522701.5:c.267G= | ENSP00000428557.1:p.Glu89= | |
ENST00000524029.5:c.267G= | ENSP00000428237.1:p.Glu89= | |
NM_000237.2:c.267G= | NP_000228.1:p.Glu89= | |
NM_000237.3:c.267G= MANE Select | NP_000228.1:p.Glu89= |