HGVS | Genome Assembly |
---|---|
NC_000010.11:g.103458411C= , CM000672.2:g.103458411C= | GRCh38 |
NC_000010.10:g.105218168C= , CM000672.1:g.105218168C= | GRCh37 |
NC_000010.9:g.105208158C= | NCBI36 |
NG_016855.1:g.5481G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000329905.6:c.341G= MANE Select | ENSP00000329926.6:p.Trp114= | |
ENST00000329905.5:c.341G= | ENSP00000329926.5:p.Trp114= | |
NM_001001412.3:c.341G= | NP_001001412.3:p.Trp114= | |
NM_001001412.4:c.341G= MANE Select | NP_001001412.3:p.Trp114= |