HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154116T>A , CM000681.2:g.55154116T>A | GRCh38 |
NC_000019.9:g.55665484T>A , CM000681.1:g.55665484T>A | GRCh37 |
NC_000019.8:g.60357296T>A | NCBI36 |
NG_007866.2:g.8617A>T , LRG_432:g.8617A>T | |
NG_011829.2:g.123A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.463A>T MANE Select | ENSP00000341838.5:p.Met155Leu | |
ENST00000665070.1:c.496A>T | ENSP00000499482.1:p.Met166Leu | |
ENST00000344887.9:c.463A>T | ENSP00000341838.5:p.Met155Leu | |
ENST00000585806.5:n.462A>T | ||
ENST00000586669.5:n.471A>T | ||
ENST00000588882.1:c.388A>T | ENSP00000466729.1:p.Met130Leu | |
ENST00000589864.1:n.291A>T | ||
NM_000363.4:c.463A>T , LRG_432t1:c.463A>T | NP_000354.4:p.Met155Leu | |
NM_000363.5:c.463A>T MANE Select | NP_000354.4:p.Met155Leu |