HGVS | Genome Assembly |
---|---|
NC_000011.10:g.124872490T>A , CM000673.2:g.124872490T>A | GRCh38 |
NC_000011.9:g.124742386T>A , CM000673.1:g.124742386T>A | GRCh37 |
NC_000011.8:g.124247596T>A | NCBI36 |
NG_016214.1:g.12082T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397801.6:c.1268T>A MANE Select | ENSP00000380903.1:p.Val423Glu | |
ENST00000397801.5:c.1268T>A | ENSP00000380903.1:p.Val423Glu | |
ENST00000538940.5:c.1202T>A | ENSP00000441797.1:p.Val401Glu | |
NM_022370.3:c.1268T>A | NP_071765.2:p.Val423Glu | |
XM_011542953.1:c.2240T>A | XP_011541255.1:p.Val747Glu | |
XM_017018122.1:c.1202T>A | XP_016873611.1:p.Val401Glu | |
NM_022370.4:c.1268T>A MANE Select | NP_071765.2:p.Val423Glu |