HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233607C>A , CM000667.2:g.55233607C>A | GRCh38 |
NC_000005.9:g.54529435C>A , CM000667.1:g.54529435C>A | GRCh37 |
NC_000005.8:g.54565192C>A | NCBI36 |
NG_034201.1:g.5111G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.-84G>T MANE Select | ENSP00000282572.4:n.-84G>T | |
ENST00000282572.4:c.-84G>T | ENSP00000282572.4:n.-84G>T | |
NM_021147.4:c.-84G>T | NP_066970.3:n.-84G>T | |
NR_125346.1:n.111G>T | ||
NR_125347.1:n.111G>T | ||
NM_021147.5:c.-84G>T MANE Select | NP_066970.3:n.-84G>T | |
NR_125346.2:n.2G>T | ||
NR_125347.2:n.2G>T |