HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94852789A>G , CM000672.2:g.94852789A>G | GRCh38 |
NC_000010.10:g.96612546A>G , CM000672.1:g.96612546A>G | GRCh37 |
NC_000010.9:g.96602536A>G | NCBI36 |
NG_008384.2:g.95084A>G | |
NG_008384.3:g.95109A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.1348A>G MANE Select | ENSP00000360372.3:p.Thr450Ala | |
ENST00000645461.1:n.2259A>G | ||
ENST00000371321.7:c.1348A>G | ENSP00000360372.3:p.Thr450Ala | |
ENST00000464755.1:c.2111A>G | ENSP00000483243.1:n.2111A>G | |
NM_000769.2:c.1348A>G | NP_000760.1:p.Thr450Ala | |
NM_000769.4:c.1348A>G MANE Select | NP_000760.1:p.Thr450Ala |