HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136659353A>G , CM000685.2:g.136659353A>G | GRCh38 |
NC_000023.10:g.135741512A>G , CM000685.1:g.135741512A>G | GRCh37 |
NC_000023.9:g.135569178A>G | NCBI36 |
NG_007280.1:g.16177A>G , LRG_141:g.16177A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*342A>G | ENSP00000512122.1:n.*342A>G | |
ENST00000695725.1:c.*279A>G | ENSP00000512123.1:n.*279A>G | |
ENST00000695726.1:n.2692A>G | ||
ENST00000695729.1:n.3527A>G | ||
ENST00000370629.7:c.724A>G MANE Select | ENSP00000359663.2:p.Thr242Ala | |
ENST00000370628.2:c.661A>G | ENSP00000359662.2:p.Thr221Ala | |
ENST00000370629.6:c.724A>G | ENSP00000359663.2:p.Thr242Ala | |
NM_000074.2:c.724A>G , LRG_141t1:c.724A>G | NP_000065.1:p.Thr242Ala | |
NM_000074.3:c.724A>G MANE Select | NP_000065.1:p.Thr242Ala |