HGVS | Genome Assembly |
---|---|
NC_000023.11:g.141895173G= , CM000685.2:g.141895173G= | GRCh38 |
NC_000023.10:g.140982959G= , CM000685.1:g.140982959G= | GRCh37 |
NC_000023.9:g.140810625G= | NCBI36 |
NG_013272.1:g.61858G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000298296.1:c.910-96G= MANE Select | ENSP00000298296.1:n.910-96G= | |
ENST00000443323.2:c.-118-1258G= | ENSP00000438254.1:n.-118-1258G= | |
ENST00000483584.5:n.150-96G= | ||
ENST00000544766.5:c.-378-96G= | ENSP00000440444.1:n.-378-96G= | |
NM_138702.1:c.910-96G= MANE Select | NP_619647.1:n.910-96G= | |
NM_177456.2:c.-378-96G= | NP_803251.1:n.-378-96G= | |
XM_011531267.1:c.-397G= | XP_011529569.1:n.-397G= | |
XM_017029265.2:c.-378-96G= | XP_016884754.1:n.-378-96G= |