HGVS | Genome Assembly |
---|---|
NC_000020.11:g.44651903T= , CM000682.2:g.44651903T= | GRCh38 |
NC_000020.10:g.43280544T= , CM000682.1:g.43280544T= | GRCh37 |
NC_000020.9:g.42713958T= | NCBI36 |
NG_007385.1:g.4833A= , LRG_16:g.4833A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000536076.2:c.-122A= | ENSP00000512234.1:n.-122A= | |
ENST00000696039.1:n.320A= | ||
ENST00000696062.1:c.96+197A= | ENSP00000512365.1:n.96+197A= | |
ENST00000696064.1:c.-119A= | ENSP00000512367.1:n.-119A= | |
ENST00000696065.1:c.-122A= | ENSP00000512368.1:n.-122A= | |
ENST00000535573.1:n.331A= | ||
ENST00000536076.1:n.212A= | ||
XM_011528479.1:c.-258A= | XP_011526781.1:n.-258A= |