HGVS | Genome Assembly |
---|---|
NC_000016.10:g.68645430C>A , CM000678.2:g.68645430C>A | GRCh38 |
NC_000016.9:g.68679333C>A , CM000678.1:g.68679333C>A | GRCh37 |
NC_000016.8:g.67236834C>A | NCBI36 |
NG_009096.1:g.6183C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264012.9:c.45+6C>A MANE Select | ENSP00000264012.4:n.45+6C>A | |
ENST00000264012.8:c.45+6C>A | ENSP00000264012.4:n.45+6C>A | |
ENST00000429102.6:c.45+6C>A | ENSP00000398485.2:n.45+6C>A | |
ENST00000542274.5:c.45+6C>A | ENSP00000464021.1:n.45+6C>A | |
NM_001793.4:c.45+6C>A | NP_001784.2:n.45+6C>A | |
XM_011522800.1:c.45+6C>A | XP_011521102.1:n.45+6C>A | |
NM_001317195.1:c.45+6C>A | NP_001304124.1:n.45+6C>A | |
NM_001317196.1:c.-6+6C>A | NP_001304125.1:n.-6+6C>A | |
NM_001793.5:c.45+6C>A | NP_001784.2:n.45+6C>A | |
XM_011522800.3:c.45+6C>A | XP_011521102.1:n.45+6C>A | |
NM_001793.6:c.45+6C>A MANE Select | NP_001784.2:n.45+6C>A | |
NM_001317195.2:c.45+6C>A | NP_001304124.1:n.45+6C>A | |
NM_001317196.2:c.-6+6C>A | NP_001304125.1:n.-6+6C>A | |
NM_001317195.3:c.45+6C>A | NP_001304124.1:n.45+6C>A |