HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233602G= , CM000667.2:g.55233602G= | GRCh38 |
NC_000005.9:g.54529430G= , CM000667.1:g.54529430G= | GRCh37 |
NC_000005.8:g.54565187G= | NCBI36 |
NG_034201.1:g.5116C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.-79C= MANE Select | ENSP00000282572.4:n.-79C= | |
ENST00000282572.4:c.-79C= | ENSP00000282572.4:n.-79C= | |
NM_021147.4:c.-79C= | NP_066970.3:n.-79C= | |
NR_125346.1:n.116C= | ||
NR_125347.1:n.116C= | ||
NM_021147.5:c.-79C= MANE Select | NP_066970.3:n.-79C= | |
NR_125346.2:n.7C= | ||
NR_125347.2:n.7C= |