HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233658T>A , CM000667.2:g.55233658T>A | GRCh38 |
NC_000005.9:g.54529486T>A , CM000667.1:g.54529486T>A | GRCh37 |
NC_000005.8:g.54565243T>A | NCBI36 |
NG_034201.1:g.5060A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.4:c.-135A>T | ENSP00000282572.4:n.-135A>T | |
NM_021147.4:c.-135A>T | NP_066970.3:n.-135A>T | |
NR_125346.1:n.60A>T | ||
NR_125347.1:n.60A>T |