HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33669056A>G , CM000668.2:g.33669056A>G | GRCh38 |
NC_000006.11:g.33636833A>G , CM000668.1:g.33636833A>G | GRCh37 |
NC_000006.10:g.33744811A>G | NCBI36 |
NG_027729.1:g.52678A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000605930.3:c.2089A>G MANE Select | ENSP00000475177.1:p.Thr697Ala | |
ENST00000374316.9:c.2089A>G | ENSP00000363435.4:p.Thr697Ala | |
ENST00000605930.2:c.2089A>G | ENSP00000475177.1:p.Thr697Ala | |
NM_002224.3:c.2089A>G | NP_002215.2:p.Thr697Ala | |
XM_011514576.1:c.2158A>G | XP_011512878.1:p.Thr720Ala | |
XM_011514577.1:c.1906A>G | XP_011512879.1:p.Thr636Ala | |
XM_011514577.3:c.1906A>G | XP_011512879.1:p.Thr636Ala | |
XM_017010832.1:c.2089A>G | XP_016866321.1:p.Thr697Ala | |
NM_002224.4:c.2089A>G MANE Select | NP_002215.2:p.Thr697Ala |