HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154047T= , CM000681.2:g.55154047T= | GRCh38 |
NC_000019.9:g.55665415T= , CM000681.1:g.55665415T= | GRCh37 |
NC_000019.8:g.60357227T= | NCBI36 |
NG_007866.2:g.8686A= , LRG_432:g.8686A= | |
NG_011829.2:g.192A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.532A= MANE Select | ENSP00000341838.5:p.Lys178= | |
ENST00000665070.1:c.565A= | ENSP00000499482.1:p.Lys189= | |
ENST00000344887.9:c.532A= | ENSP00000341838.5:p.Lys178= | |
ENST00000585806.5:n.531A= | ||
ENST00000588882.1:c.457A= | ENSP00000466729.1:p.Lys153= | |
ENST00000589864.1:n.360A= | ||
NM_000363.4:c.532A= , LRG_432t1:c.532A= | NP_000354.4:p.Lys178= | |
NM_000363.5:c.532A= MANE Select | NP_000354.4:p.Lys178= |