HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73367733C= , CM000677.2:g.73367733C= | GRCh38 |
NC_000015.9:g.73660074C= , CM000677.1:g.73660074C= | GRCh37 |
NC_000015.8:g.71447127C= | NCBI36 |
NG_009063.1:g.6532G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.538G= MANE Select | ENSP00000261917.3:p.Glu180= | |
ENST00000261917.3:c.538G= | ENSP00000261917.3:p.Glu180= | |
NM_005477.2:c.538G= | NP_005468.1:p.Glu180= | |
NM_005477.3:c.538G= MANE Select | NP_005468.1:p.Glu180= |