HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233662A>C , CM000667.2:g.55233662A>C | GRCh38 |
NC_000005.9:g.54529490A>C , CM000667.1:g.54529490A>C | GRCh37 |
NC_000005.8:g.54565247A>C | NCBI36 |
NG_034201.1:g.5056T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.4:c.-139T>G | ENSP00000282572.4:n.-139T>G | |
NM_021147.4:c.-139T>G | NP_066970.3:n.-139T>G | |
NR_125346.1:n.56T>G | ||
NR_125347.1:n.56T>G |