HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022639G>C , CM000663.2:g.17022639G>C | GRCh38 |
NC_000001.10:g.17349134G>C , CM000663.1:g.17349134G>C | GRCh37 |
NC_000001.9:g.17221721G>C | NCBI36 |
NG_012340.1:g.36532C>G , LRG_316:g.36532C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.563C>G | ENSP00000481376.2:p.Thr188Ser | |
ENST00000491274.6:c.692C>G | ENSP00000480482.2:p.Thr231Ser | |
ENST00000375499.8:c.734C>G MANE Select | ENSP00000364649.3:p.Thr245Ser | |
ENST00000375499.7:c.734C>G | ENSP00000364649.3:p.Thr245Ser | |
ENST00000475049.5:n.159C>G | ||
ENST00000485092.5:n.398C>G | ||
ENST00000485515.5:n.668C>G | ||
NM_003000.2:c.734C>G , LRG_316t1:c.734C>G | NP_002991.2:p.Thr245Ser | |
NM_003000.3:c.734C>G MANE Select | NP_002991.2:p.Thr245Ser |