HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190404780G= , CM000665.2:g.190404780G= | GRCh38 |
NC_000003.11:g.190122569G= , CM000665.1:g.190122569G= | GRCh37 |
NC_000003.10:g.191605263G= | NCBI36 |
NG_008149.1:g.21729G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264734.3:c.236G= MANE Select | ENSP00000264734.3:p.Arg79= | |
ENST00000456423.2:c.115-5123G= | ENSP00000414136.2:n.115-5123G= | |
ENST00000264734.2:c.446G= | ENSP00000264734.2:p.Arg149= | |
ENST00000456423.1:c.325-5123G= | ENSP00000414136.1:n.325-5123G= | |
ENST00000468220.1:n.428G= | ||
NM_006580.3:c.446G= | NP_006571.1:p.Arg149= | |
NM_001378492.1:c.236G= | NP_001365421.1:p.Arg79= | |
NM_001378493.1:c.236G= | NP_001365422.1:p.Arg79= | |
NM_006580.4:c.236G= MANE Select | NP_006571.2:p.Arg79= |