HGVS | Genome Assembly |
---|---|
NC_000023.11:g.141895113T>G , CM000685.2:g.141895113T>G | GRCh38 |
NC_000023.10:g.140982899T>G , CM000685.1:g.140982899T>G | GRCh37 |
NC_000023.9:g.140810565T>G | NCBI36 |
NG_013272.1:g.61798T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000298296.1:c.910-156T>G MANE Select | ENSP00000298296.1:n.910-156T>G | |
ENST00000443323.2:c.-118-1318T>G | ENSP00000438254.1:n.-118-1318T>G | |
ENST00000483584.5:n.150-156T>G | ||
ENST00000544766.5:c.-378-156T>G | ENSP00000440444.1:n.-378-156T>G | |
NM_138702.1:c.910-156T>G MANE Select | NP_619647.1:n.910-156T>G | |
NM_177456.2:c.-378-156T>G | NP_803251.1:n.-378-156T>G | |
XM_017029265.2:c.-378-156T>G | XP_016884754.1:n.-378-156T>G |