HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659137T>G , CM000685.2:g.136659137T>G | GRCh38 |
NC_000023.10:g.135741296T>G , CM000685.1:g.135741296T>G | GRCh37 |
NC_000023.9:g.135568962T>G | NCBI36 |
NG_007280.1:g.15961T>G , LRG_141:g.15961T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*126T>G | ENSP00000512122.1:n.*126T>G | |
ENST00000695725.1:c.*63T>G | ENSP00000512123.1:n.*63T>G | |
ENST00000695726.1:n.2476T>G | ||
ENST00000695729.1:n.3311T>G | ||
ENST00000370629.7:c.508T>G MANE Select | ENSP00000359663.2:p.Tyr170Asp | |
ENST00000370628.2:c.445T>G | ENSP00000359662.2:p.Tyr149Asp | |
ENST00000370629.6:c.508T>G | ENSP00000359663.2:p.Tyr170Asp | |
NM_000074.2:c.508T>G , LRG_141t1:c.508T>G | NP_000065.1:p.Tyr170Asp | |
NM_000074.3:c.508T>G MANE Select | NP_000065.1:p.Tyr170Asp |