HGVS | Genome Assembly |
---|---|
NC_000023.11:g.141895170T= , CM000685.2:g.141895170T= | GRCh38 |
NC_000023.10:g.140982956T= , CM000685.1:g.140982956T= | GRCh37 |
NC_000023.9:g.140810622T= | NCBI36 |
NG_013272.1:g.61855T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000298296.1:c.910-99T= MANE Select | ENSP00000298296.1:n.910-99T= | |
ENST00000443323.2:c.-118-1261T= | ENSP00000438254.1:n.-118-1261T= | |
ENST00000483584.5:n.150-99T= | ||
ENST00000544766.5:c.-378-99T= | ENSP00000440444.1:n.-378-99T= | |
NM_138702.1:c.910-99T= MANE Select | NP_619647.1:n.910-99T= | |
NM_177456.2:c.-378-99T= | NP_803251.1:n.-378-99T= | |
XM_011531267.1:c.-400T= | XP_011529569.1:n.-400T= | |
XM_017029265.2:c.-378-99T= | XP_016884754.1:n.-378-99T= |