HGVS | Genome Assembly |
---|---|
NC_000010.11:g.92645446G>T , CM000672.2:g.92645446G>T | GRCh38 |
NC_000010.10:g.94405203G>T , CM000672.1:g.94405203G>T | GRCh37 |
NC_000010.9:g.94395183G>T | NCBI36 |
NG_032580.1:g.57379G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260731.5:c.2351G>T MANE Select | ENSP00000260731.3:p.Arg784Ile | |
ENST00000676621.1:c.*869G>T | ENSP00000503639.1:n.*869G>T | |
ENST00000676647.1:c.2144G>T | ENSP00000503394.1:p.Arg715Ile | |
ENST00000676757.1:c.2144G>T | ENSP00000504289.1:p.Arg715Ile | |
ENST00000677720.1:c.*325G>T | ENSP00000504840.1:n.*325G>T | |
ENST00000260731.4:c.2351G>T | ENSP00000260731.3:p.Arg784Ile | |
NM_004523.3:c.2351G>T | NP_004514.2:p.Arg784Ile | |
NM_004523.4:c.2351G>T MANE Select | NP_004514.2:p.Arg784Ile |