HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571303G>A , CM000663.2:g.154571303G>A | GRCh38 |
NC_000001.10:g.154543779G>A , CM000663.1:g.154543779G>A | GRCh37 |
NC_000001.9:g.152810403G>A | NCBI36 |
NG_008027.1:g.8523G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.480G>A MANE Select | ENSP00000357461.3:p.Lys160= | |
ENST00000636034.1:c.480G>A | ENSP00000489703.1:p.Lys160= | |
ENST00000637900.1:c.486G>A | ENSP00000490474.1:p.Lys162= | |
ENST00000368476.3:c.480G>A | ENSP00000357461.3:p.Lys160= | |
NM_000748.2:c.480G>A | NP_000739.1:p.Lys160= | |
XM_017000180.2:c.-9-22G>A | XP_016855669.1:n.-9-22G>A | |
XR_001736952.2:n.732G>A | ||
NM_000748.3:c.480G>A MANE Select | NP_000739.1:p.Lys160= |