HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31667284C>G , CM000683.2:g.31667284C>G | GRCh38 |
NC_000021.8:g.33039597C>G , CM000683.1:g.33039597C>G | GRCh37 |
NC_000021.7:g.31961468C>G | NCBI36 |
NG_008689.1:g.12663C>G , LRG_652:g.12663C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.266C>G MANE Select | ENSP00000270142.7:p.Thr89Ser | |
ENST00000270142.10:c.266C>G | ENSP00000270142.6:p.Thr89Ser | |
ENST00000389995.4:c.209C>G | ENSP00000374645.4:p.Thr70Ser | |
ENST00000470944.1:n.1194C>G | ||
ENST00000476106.5:n.529C>G | ||
NM_000454.4:c.266C>G , LRG_652t1:c.266C>G | NP_000445.1:p.Thr89Ser | |
NM_000454.5:c.266C>G MANE Select | NP_000445.1:p.Thr89Ser |