HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44351762G= , CM000679.2:g.44351762G= | GRCh38 |
NC_000017.10:g.42429130G= , CM000679.1:g.42429130G= | GRCh37 |
NC_000017.9:g.39784656G= | NCBI36 |
NG_007886.1:g.11640G= , LRG_661:g.11640G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000053867.8:c.1146G= MANE Select | ENSP00000053867.2:p.Thr382= | |
ENST00000639447.1:c.1136+10G= | ENSP00000492014.1:n.1136+10G= | |
ENST00000053867.7:c.1146G= | ENSP00000053867.2:p.Thr382= | |
ENST00000586443.1:c.587G= | ||
ENST00000589265.5:c.675G= | ENSP00000467616.1:p.Thr225= | |
ENST00000589923.1:n.404G= | ||
NM_002087.3:c.1146G= | NP_002078.1:p.Thr382= | |
XM_005257253.1:c.1146G= | XP_005257310.1:p.Thr382= | |
XM_024450730.1:c.1146G= | XP_024306498.1:p.Thr382= | |
NM_002087.4:c.1146G= MANE Select | NP_002078.1:p.Thr382= |