HGVS | Genome Assembly |
---|---|
NC_000013.11:g.53051661G= , CM000675.2:g.53051661G= | GRCh38 |
NC_000013.10:g.53625796G= , CM000675.1:g.53625796G= | GRCh37 |
NC_000013.9:g.52523797G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000219022.3:c.*890G= MANE Select | ENSP00000219022.2:n.*890G= | |
ENST00000219022.2:c.*890G= | ENSP00000219022.2:n.*890G= | |
NM_006418.4:c.*890G= | NP_006409.3:n.*890G= | |
NM_006418.5:c.*890G= MANE Select | NP_006409.3:n.*890G= |