HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233235T>C , CM000667.2:g.55233235T>C | GRCh38 |
NC_000005.9:g.54529063T>C , CM000667.1:g.54529063T>C | GRCh37 |
NC_000005.8:g.54564820T>C | NCBI36 |
NG_034201.1:g.5483A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.289A>G MANE Select | ENSP00000282572.4:p.Thr97Ala | |
ENST00000282572.4:c.289A>G | ENSP00000282572.4:p.Thr97Ala | |
ENST00000501463.2:c.289A>G | ENSP00000422485.1:p.Thr97Ala | |
NM_021147.4:c.289A>G | NP_066970.3:p.Thr97Ala | |
NR_125346.1:n.483A>G | ||
NR_125347.1:n.483A>G | ||
NM_021147.5:c.289A>G MANE Select | NP_066970.3:p.Thr97Ala | |
NR_125346.2:n.374A>G | ||
NR_125347.2:n.374A>G |