HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133538797G>T , CM000672.2:g.133538797G>T | GRCh38 |
NC_000010.10:g.135352301G>T , CM000672.1:g.135352301G>T | GRCh37 |
NC_000010.9:g.135202291G>T | NCBI36 |
NG_008383.1:g.16435G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252945.8:c.1315G>T MANE Select | ENSP00000252945.3:p.Gly439Ter | |
ENST00000252945.7:c.1315G>T | ENSP00000252945.3:p.Gly439Ter | |
ENST00000368520.1:n.1358+905G>T | ||
ENST00000418356.1:c.904G>T | ENSP00000397299.1:p.Gly302Ter | |
ENST00000421586.5:c.1054G>T | ENSP00000412754.1:p.Gly352Ter | |
ENST00000463117.6:c.1315G>T | ENSP00000440689.1:p.Gly439Ter | |
ENST00000469258.1:n.411G>T | ||
ENST00000541080.5:c.731G>T | ||
NM_000773.3:c.1315G>T | NP_000764.1:p.Gly439Ter | |
NM_000773.4:c.1315G>T MANE Select | NP_000764.1:p.Gly439Ter |