HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24145731A= , CM000668.2:g.24145731A= | GRCh38 |
NC_000006.11:g.24145959A= , CM000668.1:g.24145959A= | GRCh37 |
NC_000006.10:g.24253938A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378491.9:c.373A= MANE Select | ENSP00000367752.4:p.Ile125= | |
ENST00000378477.2:c.373A= | ENSP00000367738.2:p.Ile125= | |
ENST00000378478.5:c.373A= | ENSP00000367739.2:p.Ile125= | |
ENST00000378491.8:c.373A= | ENSP00000367752.4:p.Ile125= | |
ENST00000468195.2:n.257-9040A= | ||
NM_080723.4:c.373A= | NP_542454.3:p.Ile125= | |
NM_080723.5:c.373A= MANE Select | NP_542454.3:p.Ile125= |