HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225800C>A , CM000668.2:g.3225800C>A | GRCh38 |
NC_000006.11:g.3226034C>A , CM000668.1:g.3226034C>A | GRCh37 |
NC_000006.10:g.3171033C>A | NCBI36 |
NG_016715.1:g.6935G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.289G>T MANE Select | ENSP00000259818.6:p.Ala97Ser | |
ENST00000680070.1:n.1219G>T | ||
ENST00000681707.1:n.1116G>T | ||
ENST00000681757.1:n.594G>T | ||
ENST00000259818.7:c.289G>T | ENSP00000259818.6:p.Ala97Ser | |
ENST00000473006.1:n.406G>T | ||
NM_178012.4:c.289G>T | NP_821080.1:p.Ala97Ser | |
XM_011514571.1:c.73G>T | XP_011512873.1:p.Ala25Ser | |
NM_178012.5:c.289G>T MANE Select | NP_821080.1:p.Ala97Ser |