HGVS | Genome Assembly |
---|---|
NC_000023.11:g.139537156G= , CM000685.2:g.139537156G= | GRCh38 |
NC_000023.10:g.138619315G= , CM000685.1:g.138619315G= | GRCh37 |
NC_000023.9:g.138446981G= | NCBI36 |
NG_007994.1:g.11421G= , LRG_556:g.11421G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000218099.7:c.235G= MANE Select | ENSP00000218099.2:p.Glu79= | |
ENST00000218099.6:c.235G= | ENSP00000218099.2:p.Glu79= | |
ENST00000394090.2:c.235G= | ENSP00000377650.2:p.Glu79= | |
ENST00000479617.2:n.241+1G= | ||
NM_000133.3:c.235G= , LRG_556t1:c.235G= | NP_000124.1:p.Glu79= | |
NM_001313913.1:c.235G= | NP_001300842.1:p.Glu79= | |
XM_005262397.3:c.235G= | XP_005262454.1:p.Glu79= | |
XM_005262397.4:c.235G= | XP_005262454.1:p.Glu79= | |
NM_000133.4:c.235G= MANE Select | NP_000124.1:p.Glu79= | |
NM_001313913.2:c.235G= | NP_001300842.1:p.Glu79= |