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