HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131890445A= , CM000668.2:g.131890445A= | GRCh38 |
NC_000006.11:g.132211585A= , CM000668.1:g.132211585A= | GRCh37 |
NC_000006.10:g.132253278A= | NCBI36 |
NG_008206.1:g.87430A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684674.1:n.1143A= | ||
ENST00000647893.1:c.2712A= MANE Select | ENSP00000498074.1:p.Arg904= | |
ENST00000360971.6:c.2712A= | ENSP00000354238.2:p.Arg904= | |
ENST00000513998.5:c.*1549A= | ENSP00000422424.1:n.*1549A= | |
NM_006208.2:c.2712A= | NP_006199.2:p.Arg904= | |
XM_011535896.1:c.1602A= | XP_011534198.1:p.Arg534= | |
NM_006208.3:c.2712A= MANE Select | NP_006199.2:p.Arg904= |