HGVS | Genome Assembly |
---|---|
NC_000021.9:g.34370705G= , CM000683.2:g.34370705G= | GRCh38 |
NC_000021.8:g.35743004G= , CM000683.1:g.35743004G= | GRCh37 |
NC_000021.7:g.34664874G= | NCBI36 |
NG_008804.1:g.11682G= , LRG_291:g.11682G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000290310.4:c.227G= MANE Select | ENSP00000290310.2:p.Arg76= | |
ENST00000290310.3:c.227G= | ENSP00000290310.2:p.Arg76= | |
NM_172201.1:c.227G= , LRG_291t1:c.227G= | NP_751951.1:p.Arg76= | |
XR_937683.1:n.616C= | ||
XR_937684.1:n.616C= | ||
XR_001755012.2:n.737C= | ||
XR_001755013.2:n.616C= | ||
XR_937683.2:n.616C= | ||
NM_172201.2:c.227G= MANE Select | NP_751951.1:p.Arg76= |