HGVS | Genome Assembly |
---|---|
NC_000011.10:g.17553474C= , CM000673.2:g.17553474C= | GRCh38 |
NC_000011.9:g.17575021C= , CM000673.1:g.17575021C= | GRCh37 |
NC_000011.8:g.17531597C= | NCBI36 |
NG_033191.1:g.11102C= | |
NG_033191.2:g.11102C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000399391.7:c.531C= | ENSP00000382323.2:p.Thr177= | |
ENST00000399397.6:c.495C= MANE Select | ENSP00000382329.2:p.Thr165= | |
ENST00000399391.6:c.531C= | ENSP00000382323.2:p.Thr177= | |
ENST00000399397.5:c.495C= | ENSP00000382329.2:p.Thr165= | |
ENST00000498332.5:n.401C= | ||
NM_001277269.1:c.531C= | NP_001264198.1:p.Thr177= | |
NM_001292063.1:c.495C= | NP_001278992.1:p.Thr165= | |
NM_001277269.2:c.531C= | NP_001264198.1:p.Thr177= | |
NM_001292063.2:c.495C= MANE Select | NP_001278992.1:p.Thr165= |