HGVS | Genome Assembly |
---|---|
NC_000023.11:g.43949973C>A , CM000685.2:g.43949973C>A | GRCh38 |
NC_000023.10:g.43809219C>A , CM000685.1:g.43809219C>A | GRCh37 |
NC_000023.9:g.43694163C>A | NCBI36 |
NG_009832.1:g.28703G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000642620.1:c.228G>T (NDP) MANE Select | ENSP00000495972.1:p.Glu76Asp | |
ENST00000647044.1:c.228G>T (NDP) | ENSP00000495811.1:p.Glu76Asp | |
ENST00000378062.5:c.228G>T (NDP) | ENSP00000367301.5:p.Glu76Asp | |
ENST00000470584.1:n.272G>T (NDP) | ||
NM_000266.3:c.228G>T (NDP) | NP_000257.1:p.Glu76Asp | |
NR_046631.1:n.242C>A (NDP-AS1) | ||
NM_000266.4:c.228G>T (NDP) MANE Select | NP_000257.1:p.Glu76Asp |