HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2445409C>G , CM000673.2:g.2445409C>G | GRCh38 |
NC_000011.9:g.2466639C>G , CM000673.1:g.2466639C>G | GRCh37 |
NC_000011.8:g.2423215C>G | NCBI36 |
NG_008935.1:g.5419C>G , LRG_287:g.5419C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000496887.7:c.50C>G | ENSP00000434560.2:p.Thr17Ser | |
ENST00000646564.2:c.311C>G | ENSP00000495806.2:p.Thr104Ser | |
ENST00000155840.12:c.311C>G MANE Select | ENSP00000155840.2:p.Thr104Ser | |
ENST00000155840.9:c.311C>G | ENSP00000155840.2:p.Thr104Ser | |
ENST00000345015.4:n.88C>G | ||
ENST00000496887.6:c.50C>G | ENSP00000434560.1:p.Thr17Ser | |
NM_000218.2:c.311C>G , LRG_287t1:c.311C>G | NP_000209.2:p.Thr104Ser | |
NM_000218.3:c.311C>G MANE Select | NP_000209.2:p.Thr104Ser |