HGVS | Genome Assembly |
---|---|
NC_000020.11:g.49906167T>C , CM000682.2:g.49906167T>C | GRCh38 |
NC_000020.10:g.48522704T>C , CM000682.1:g.48522704T>C | GRCh37 |
NC_000020.9:g.47956111T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289431.10:c.1015A>G MANE Select | ENSP00000289431.5:p.Thr339Ala | |
ENST00000289431.9:c.1015A>G | ENSP00000289431.5:p.Thr339Ala | |
ENST00000422556.1:c.1015A>G | ENSP00000416799.1:p.Thr339Ala | |
NM_001135773.1:c.1015A>G | NP_001129245.1:p.Thr339Ala | |
NM_006038.3:c.1015A>G | NP_006029.1:p.Thr339Ala | |
XM_006723894.1:c.1015A>G | XP_006723957.1:p.Thr339Ala | |
XM_011529116.1:c.1015A>G | XP_011527418.1:p.Thr339Ala | |
NM_006038.4:c.1015A>G MANE Select | NP_006029.1:p.Thr339Ala | |
NM_001135773.2:c.1015A>G | NP_001129245.1:p.Thr339Ala |