HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022705C>G , CM000663.2:g.17022705C>G | GRCh38 |
NC_000001.10:g.17349200C>G , CM000663.1:g.17349200C>G | GRCh37 |
NC_000001.9:g.17221787C>G | NCBI36 |
NG_012340.1:g.36466G>C , LRG_316:g.36466G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.497G>C | ENSP00000481376.2:p.Arg166Thr | |
ENST00000491274.6:c.626G>C | ENSP00000480482.2:p.Arg209Thr | |
ENST00000375499.8:c.668G>C MANE Select | ENSP00000364649.3:p.Arg223Thr | |
ENST00000375499.7:c.668G>C | ENSP00000364649.3:p.Arg223Thr | |
ENST00000475049.5:n.93G>C | ||
ENST00000485092.5:n.332G>C | ||
ENST00000485515.5:n.602G>C | ||
NM_003000.2:c.668G>C , LRG_316t1:c.668G>C | NP_002991.2:p.Arg223Thr | |
NM_003000.3:c.668G>C MANE Select | NP_002991.2:p.Arg223Thr |