HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151774T>C , CM000681.2:g.55151774T>C | GRCh38 |
NC_000019.9:g.55663142T>C , CM000681.1:g.55663142T>C | GRCh37 |
NC_000019.8:g.60354954T>C | NCBI36 |
NG_007866.2:g.10959A>G , LRG_432:g.10959A>G | |
NG_011829.2:g.2465A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.*60A>G MANE Select | ENSP00000341838.5:n.*60A>G | |
ENST00000665070.1:c.*60A>G | ENSP00000499482.1:n.*60A>G | |
ENST00000344887.9:c.*60A>G | ENSP00000341838.5:n.*60A>G | |
ENST00000585806.5:n.692A>G | ||
ENST00000588882.1:c.*60A>G | ENSP00000466729.1:n.*60A>G | |
ENST00000589864.1:n.521A>G | ||
NM_000363.4:c.*60A>G , LRG_432t1:c.*60A>G | NP_000354.4:n.*60A>G | |
NM_000363.5:c.*60A>G MANE Select | NP_000354.4:n.*60A>G |