HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233531C>A , CM000667.2:g.55233531C>A | GRCh38 |
NC_000005.9:g.54529359C>A , CM000667.1:g.54529359C>A | GRCh37 |
NC_000005.8:g.54565116C>A | NCBI36 |
NG_034201.1:g.5187G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.-8G>T MANE Select | ENSP00000282572.4:n.-8G>T | |
ENST00000282572.4:c.-8G>T | ENSP00000282572.4:n.-8G>T | |
ENST00000501463.2:c.-8G>T | ENSP00000422485.1:n.-8G>T | |
NM_021147.4:c.-8G>T | NP_066970.3:n.-8G>T | |
NR_125346.1:n.187G>T | ||
NR_125347.1:n.187G>T | ||
NM_021147.5:c.-8G>T MANE Select | NP_066970.3:n.-8G>T | |
NR_125346.2:n.78G>T | ||
NR_125347.2:n.78G>T |