HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659063A>T , CM000685.2:g.136659063A>T | GRCh38 |
NC_000023.10:g.135741222A>T , CM000685.1:g.135741222A>T | GRCh37 |
NC_000023.9:g.135568888A>T | NCBI36 |
NG_007280.1:g.15887A>T , LRG_141:g.15887A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*52A>T | ENSP00000512122.1:n.*52A>T | |
ENST00000695725.1:c.181A>T | ENSP00000512123.1:p.Thr61Ser | |
ENST00000695726.1:n.2402A>T | ||
ENST00000695729.1:n.3237A>T | ||
ENST00000370629.7:c.434A>T MANE Select | ENSP00000359663.2:p.Tyr145Phe | |
ENST00000370628.2:c.371A>T | ENSP00000359662.2:p.Tyr124Phe | |
ENST00000370629.6:c.434A>T | ENSP00000359663.2:p.Tyr145Phe | |
NM_000074.2:c.434A>T , LRG_141t1:c.434A>T | NP_000065.1:p.Tyr145Phe | |
NM_000074.3:c.434A>T MANE Select | NP_000065.1:p.Tyr145Phe |