HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44352198A= , CM000679.2:g.44352198A= | GRCh38 |
NC_000017.10:g.42429566A= , CM000679.1:g.42429566A= | GRCh37 |
NC_000017.9:g.39785092A= | NCBI36 |
NG_007886.1:g.12076A= , LRG_661:g.12076A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000053867.8:c.1363A= MANE Select | ENSP00000053867.2:p.Thr455= | |
ENST00000639447.1:c.1137-331A= | ENSP00000492014.1:n.1137-331A= | |
ENST00000053867.7:c.1363A= | ENSP00000053867.2:p.Thr455= | |
ENST00000586443.1:c.804A= | ||
ENST00000589265.5:c.892A= | ENSP00000467616.1:p.Thr298= | |
NM_002087.3:c.1363A= | NP_002078.1:p.Thr455= | |
XM_005257253.1:c.1363A= | XP_005257310.1:p.Thr455= | |
XM_024450730.1:c.1363A= | XP_024306498.1:p.Thr455= | |
NM_002087.4:c.1363A= MANE Select | NP_002078.1:p.Thr455= |