HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81646413G>C , CM000665.2:g.81646413G>C | GRCh38 |
NC_000003.11:g.81695564G>C , CM000665.1:g.81695564G>C | GRCh37 |
NC_000003.10:g.81778254G>C | NCBI36 |
NG_011810.1:g.120388C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.761C>G MANE Select | ENSP00000410833.2:p.Thr254Arg | |
ENST00000429644.6:c.761C>G | ENSP00000410833.2:p.Thr254Arg | |
ENST00000489715.1:c.638C>G | ENSP00000419638.1:p.Thr213Arg | |
ENST00000498468.1:n.311C>G | ||
NM_000158.3:c.761C>G | NP_000149.3:p.Thr254Arg | |
NM_000158.4:c.761C>G MANE Select | NP_000149.4:p.Thr254Arg |