HGVS | Genome Assembly |
---|---|
NC_000016.10:g.1985894A>G , CM000678.2:g.1985894A>G | GRCh38 |
NC_000016.9:g.2035895A>G , CM000678.1:g.2035895A>G | GRCh37 |
NC_000016.8:g.1975896A>G | NCBI36 |
NG_016288.1:g.6746A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000567719.2:c.259A>G | ENSP00000455885.1:p.Thr87Ala | |
ENST00000248114.7:c.484A>G MANE Select | ENSP00000248114.6:p.Thr162Ala | |
ENST00000248114.6:c.484A>G | ENSP00000248114.6:p.Thr162Ala | |
ENST00000565658.1:n.641A>G | ||
ENST00000567719.1:c.259A>G | ENSP00000455885.1:p.Thr87Ala | |
ENST00000569451.1:c.287A>G | ENSP00000456432.1:p.His96Arg | |
NM_005262.2:c.484A>G | NP_005253.3:p.Thr162Ala | |
NM_005262.3:c.484A>G MANE Select | NP_005253.3:p.Thr162Ala |