HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56042018G= , CM000674.2:g.56042018G= | GRCh38 |
NC_000012.11:g.56435802G= , CM000674.1:g.56435802G= | GRCh37 |
NC_000012.10:g.54722069G= | NCBI36 |
NG_023201.1:g.5117G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356464.10:c.-149G= | ENSP00000348849.5:n.-149G= | |
ENST00000646449.2:c.-149G= MANE Select | ENSP00000496643.1:n.-149G= | |
ENST00000356464.9:c.-149G= | ENSP00000348849.5:n.-149G= | |
ENST00000552361.1:c.-81G= | ENSP00000450339.1:n.-81G= | |
NM_001029.3:c.-149G= | NP_001020.2:n.-149G= | |
NM_001029.5:c.-149G= MANE Select | NP_001020.2:n.-149G= |