HGVS | Genome Assembly |
---|---|
NC_000006.12:g.121447333G= , CM000668.2:g.121447333G= | GRCh38 |
NC_000006.11:g.121768479G= , CM000668.1:g.121768479G= | GRCh37 |
NC_000006.10:g.121810178G= | NCBI36 |
NG_008308.1:g.16735G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000282561.4:c.486G= MANE Select | ENSP00000282561.3:p.Lys162= | |
ENST00000647564.1:c.486G= | ENSP00000497565.1:p.Lys162= | |
ENST00000649003.1:c.486G= | ENSP00000497283.1:p.Lys162= | |
ENST00000650427.1:c.486G= | ENSP00000497367.1:p.Lys162= | |
ENST00000282561.3:c.486G= | ENSP00000282561.3:p.Lys162= | |
NM_000165.4:c.486G= | NP_000156.1:p.Lys162= | |
NM_000165.5:c.486G= MANE Select | NP_000156.1:p.Lys162= |