HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56042070T= , CM000674.2:g.56042070T= | GRCh38 |
NC_000012.11:g.56435854T= , CM000674.1:g.56435854T= | GRCh37 |
NC_000012.10:g.54722121T= | NCBI36 |
NG_023201.1:g.5169T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000356464.10:c.-97T= | ENSP00000348849.5:n.-97T= | |
ENST00000646449.2:c.-97T= MANE Select | ENSP00000496643.1:n.-97T= | |
ENST00000356464.9:c.-97T= | ENSP00000348849.5:n.-97T= | |
ENST00000552361.1:c.-35+6T= | ENSP00000450339.1:n.-35+6T= | |
NM_001029.3:c.-97T= | NP_001020.2:n.-97T= | |
NM_001029.5:c.-97T= MANE Select | NP_001020.2:n.-97T= |