HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154068C= , CM000681.2:g.55154068C= | GRCh38 |
NC_000019.9:g.55665436C= , CM000681.1:g.55665436C= | GRCh37 |
NC_000019.8:g.60357248C= | NCBI36 |
NG_007866.2:g.8665G= , LRG_432:g.8665G= | |
NG_011829.2:g.171G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.511G= MANE Select | ENSP00000341838.5:p.Ala171= | |
ENST00000665070.1:c.544G= | ENSP00000499482.1:p.Ala182= | |
ENST00000344887.9:c.511G= | ENSP00000341838.5:p.Ala171= | |
ENST00000585806.5:n.510G= | ||
ENST00000588882.1:c.436G= | ENSP00000466729.1:p.Ala146= | |
ENST00000589864.1:n.339G= | ||
NM_000363.4:c.511G= , LRG_432t1:c.511G= | NP_000354.4:p.Ala171= | |
NM_000363.5:c.511G= MANE Select | NP_000354.4:p.Ala171= |