HGVS | Genome Assembly |
---|---|
NC_000011.10:g.17642166T>C , CM000673.2:g.17642166T>C | GRCh38 |
NC_000011.9:g.17663713T>C , CM000673.1:g.17663713T>C | GRCh37 |
NC_000011.8:g.17620289T>C | NCBI36 |
NG_033191.1:g.99794T>C | |
NG_033191.2:g.99794T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000399391.7:c.8371T>C | ENSP00000382323.2:p.Cys2791Arg | |
ENST00000399397.6:c.8335T>C MANE Select | ENSP00000382329.2:p.Cys2779Arg | |
ENST00000399391.6:c.8371T>C | ENSP00000382323.2:p.Cys2791Arg | |
ENST00000399397.5:c.8335T>C | ENSP00000382329.2:p.Cys2779Arg | |
NM_001277269.1:c.8371T>C | NP_001264198.1:p.Cys2791Arg | |
NM_001292063.1:c.8335T>C | NP_001278992.1:p.Cys2779Arg | |
NM_001277269.2:c.8371T>C | NP_001264198.1:p.Cys2791Arg | |
NM_001292063.2:c.8335T>C MANE Select | NP_001278992.1:p.Cys2779Arg |