HGVS | Genome Assembly |
---|---|
NC_000022.11:g.43946248G>A , CM000684.2:g.43946248G>A | GRCh38 |
NC_000022.10:g.44342128G>A , CM000684.1:g.44342128G>A | GRCh37 |
NC_000022.9:g.42673461G>A | NCBI36 |
NG_008631.1:g.27510G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216180.8:c.1312G>A MANE Select | ENSP00000216180.3:p.Ala438Thr | |
ENST00000216180.7:c.1312G>A | ENSP00000216180.3:p.Ala438Thr | |
ENST00000406117.6:c.*849+1453G>A | ENSP00000384668.2:n.*849+1453G>A | |
ENST00000423180.2:c.1300G>A | ENSP00000397987.2:p.Ala434Thr | |
NM_025225.2:c.1312G>A | NP_079501.2:p.Ala438Thr | |
NM_025225.3:c.1312G>A MANE Select | NP_079501.2:p.Ala438Thr |