HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154074G>A , CM000681.2:g.55154074G>A | GRCh38 |
NC_000019.9:g.55665442G>A , CM000681.1:g.55665442G>A | GRCh37 |
NC_000019.8:g.60357254G>A | NCBI36 |
NG_007866.2:g.8659C>T , LRG_432:g.8659C>T | |
NG_011829.2:g.165C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.505C>T MANE Select | ENSP00000341838.5:p.Leu169= | |
ENST00000665070.1:c.538C>T | ENSP00000499482.1:p.Leu180= | |
ENST00000344887.9:c.505C>T | ENSP00000341838.5:p.Leu169= | |
ENST00000585806.5:n.504C>T | ||
ENST00000588882.1:c.430C>T | ENSP00000466729.1:p.Leu144= | |
ENST00000589864.1:n.333C>T | ||
NM_000363.4:c.505C>T , LRG_432t1:c.505C>T | NP_000354.4:p.Leu169= | |
NM_000363.5:c.505C>T MANE Select | NP_000354.4:p.Leu169= |