HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160128789C= , CM000663.2:g.160128789C= | GRCh38 |
NC_000001.10:g.160098579C= , CM000663.1:g.160098579C= | GRCh37 |
NC_000001.9:g.158365203C= | NCBI36 |
NG_008014.1:g.18032C= , LRG_6:g.18032C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361216.8:c.1155C= MANE Select | ENSP00000354490.3:p.Thr385= | |
ENST00000361216.7:c.1155C= | ENSP00000354490.3:p.Thr385= | |
ENST00000392233.7:c.1155C= | ENSP00000376066.3:p.Thr385= | |
ENST00000447527.1:c.287C= | ||
ENST00000472488.5:n.1258C= | ||
NM_000702.3:c.1155C= | NP_000693.1:p.Thr385= | |
NM_000702.4:c.1155C= MANE Select | NP_000693.1:p.Thr385= |