HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233479T>A , CM000667.2:g.55233479T>A | GRCh38 |
NC_000005.9:g.54529307T>A , CM000667.1:g.54529307T>A | GRCh37 |
NC_000005.8:g.54565064T>A | NCBI36 |
NG_034201.1:g.5239A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.45A>T MANE Select | ENSP00000282572.4:p.Arg15= | |
ENST00000282572.4:c.45A>T | ENSP00000282572.4:p.Arg15= | |
ENST00000501463.2:c.45A>T | ENSP00000422485.1:p.Arg15= | |
NM_021147.4:c.45A>T | NP_066970.3:p.Arg15= | |
NR_125346.1:n.239A>T | ||
NR_125347.1:n.239A>T | ||
NM_021147.5:c.45A>T MANE Select | NP_066970.3:p.Arg15= | |
NR_125346.2:n.130A>T | ||
NR_125347.2:n.130A>T |