HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154071G= , CM000681.2:g.55154071G= | GRCh38 |
NC_000019.9:g.55665439G= , CM000681.1:g.55665439G= | GRCh37 |
NC_000019.8:g.60357251G= | NCBI36 |
NG_007866.2:g.8662C= , LRG_432:g.8662C= | |
NG_011829.2:g.168C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.508C= MANE Select | ENSP00000341838.5:p.Arg170= | |
ENST00000665070.1:c.541C= | ENSP00000499482.1:p.Arg181= | |
ENST00000344887.9:c.508C= | ENSP00000341838.5:p.Arg170= | |
ENST00000585806.5:n.507C= | ||
ENST00000588882.1:c.433C= | ENSP00000466729.1:p.Arg145= | |
ENST00000589864.1:n.336C= | ||
NM_000363.4:c.508C= , LRG_432t1:c.508C= | NP_000354.4:p.Arg170= | |
NM_000363.5:c.508C= MANE Select | NP_000354.4:p.Arg170= |