HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571416C>G , CM000663.2:g.154571416C>G | GRCh38 |
NC_000001.10:g.154543892C>G , CM000663.1:g.154543892C>G | GRCh37 |
NC_000001.9:g.152810516C>G | NCBI36 |
NG_008027.1:g.8636C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.593C>G MANE Select | ENSP00000357461.3:p.Thr198Arg | |
ENST00000636034.1:c.593C>G | ENSP00000489703.1:p.Thr198Arg | |
ENST00000637900.1:c.599C>G | ENSP00000490474.1:p.Thr200Arg | |
ENST00000368476.3:c.593C>G | ENSP00000357461.3:p.Thr198Arg | |
NM_000748.2:c.593C>G | NP_000739.1:p.Thr198Arg | |
XM_017000180.2:c.83C>G | XP_016855669.1:p.Thr28Arg | |
XR_001736952.2:n.845C>G | ||
NM_000748.3:c.593C>G MANE Select | NP_000739.1:p.Thr198Arg |