HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659084T>A , CM000685.2:g.136659084T>A | GRCh38 |
NC_000023.10:g.135741243T>A , CM000685.1:g.135741243T>A | GRCh37 |
NC_000023.9:g.135568909T>A | NCBI36 |
NG_007280.1:g.15908T>A , LRG_141:g.15908T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*73T>A | ENSP00000512122.1:n.*73T>A | |
ENST00000695725.1:c.*10T>A | ENSP00000512123.1:n.*10T>A | |
ENST00000695726.1:n.2423T>A | ||
ENST00000695729.1:n.3258T>A | ||
ENST00000370629.7:c.455T>A MANE Select | ENSP00000359663.2:p.Leu152Ter | |
ENST00000370628.2:c.392T>A | ENSP00000359662.2:p.Leu131Ter | |
ENST00000370629.6:c.455T>A | ENSP00000359663.2:p.Leu152Ter | |
NM_000074.2:c.455T>A , LRG_141t1:c.455T>A | NP_000065.1:p.Leu152Ter | |
NM_000074.3:c.455T>A MANE Select | NP_000065.1:p.Leu152Ter |