HGVS | Genome Assembly |
---|---|
NC_000020.11:g.23637704C= , CM000682.2:g.23637704C= | GRCh38 |
NC_000020.10:g.23618341C= , CM000682.1:g.23618341C= | GRCh37 |
NC_000020.9:g.23566341C= | NCBI36 |
NG_012887.2:g.5234G= | |
NG_012887.3:g.5234G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376925.8:c.159G= MANE Select | ENSP00000366124.3:p.Leu53= | |
ENST00000376925.7:c.159G= | ENSP00000366124.3:p.Leu53= | |
ENST00000398409.1:c.159G= | ENSP00000381446.1:p.Leu53= | |
ENST00000398411.5:c.159G= | ENSP00000381448.1:p.Leu53= | |
NM_000099.3:c.159G= | NP_000090.1:p.Leu53= | |
NM_001288614.1:c.159G= | NP_001275543.1:p.Leu53= | |
NM_000099.4:c.159G= MANE Select | NP_000090.1:p.Leu53= | |
NM_001288614.2:c.159G= | NP_001275543.1:p.Leu53= |