HGVS | Genome Assembly |
---|---|
NC_000023.11:g.46853641A= , CM000685.2:g.46853641A= | GRCh38 |
NC_000023.10:g.46713076A= , CM000685.1:g.46713076A= | GRCh37 |
NC_000023.9:g.46598020A= | NCBI36 |
NG_009107.1:g.21730A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218340.4:c.268A= MANE Select | ENSP00000218340.3:p.Ile90= | |
ENST00000218340.3:c.268A= | ENSP00000218340.3:p.Ile90= | |
NM_006915.2:c.268A= | NP_008846.2:p.Ile90= | |
NM_006915.3:c.268A= MANE Select | NP_008846.2:p.Ile90= |