HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136648293T>G , CM000685.2:g.136648293T>G | GRCh38 |
NC_000023.10:g.135730452T>G , CM000685.1:g.135730452T>G | GRCh37 |
NC_000023.9:g.135558118T>G | NCBI36 |
NG_007280.1:g.5117T>G , LRG_141:g.5117T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.45T>G | ENSP00000512122.1:p.Thr15= | |
ENST00000695725.1:c.45T>G | ENSP00000512123.1:p.Thr15= | |
ENST00000695726.1:n.88T>G | ||
ENST00000695727.1:n.32T>G | ||
ENST00000695728.1:n.32T>G | ||
ENST00000370629.7:c.45T>G MANE Select | ENSP00000359663.2:p.Thr15= | |
ENST00000370628.2:c.45T>G | ENSP00000359662.2:p.Thr15= | |
ENST00000370629.6:c.45T>G | ENSP00000359663.2:p.Thr15= | |
NM_000074.2:c.45T>G , LRG_141t1:c.45T>G | NP_000065.1:p.Thr15= | |
NM_000074.3:c.45T>G MANE Select | NP_000065.1:p.Thr15= |