HGVS | Genome Assembly |
---|---|
NC_000001.11:g.42927755C= , CM000663.2:g.42927755C= | GRCh38 |
NC_000001.10:g.43393426C= , CM000663.1:g.43393426C= | GRCh37 |
NC_000001.9:g.43166013C= | NCBI36 |
NG_008232.1:g.36422G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000426263.10:c.1128G= MANE Select | ENSP00000416293.2:p.Val376= | |
ENST00000674545.1:n.1745G= | ||
ENST00000674765.1:c.1030-898G= | ENSP00000501811.1:n.1030-898G= | |
ENST00000675112.1:n.1429G= | ||
ENST00000676254.1:n.1577G= | ||
ENST00000426263.7:c.1128G= | ENSP00000416293.2:p.Val376= | |
ENST00000475162.3:c.416-777G= | ||
ENST00000630287.2:c.*443G= | ENSP00000486694.1:n.*443G= | |
NM_006516.2:c.1128G= | NP_006507.2:p.Val376= | |
NM_006516.3:c.1128G= | NP_006507.2:p.Val376= | |
NM_006516.4:c.1128G= MANE Select | NP_006507.2:p.Val376= |