HGVS | Genome Assembly |
---|---|
NC_000021.9:g.36146334A= , CM000683.2:g.36146334A= | GRCh38 |
NC_000021.8:g.37518632A= , CM000683.1:g.37518632A= | GRCh37 |
NC_000021.7:g.36440502A= | NCBI36 |
NG_052818.1:g.16434A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000290354.6:c.656A= (CBR3) MANE Select | ENSP00000290354.5:p.Asp219= | |
ENST00000290354.5:c.656A= (CBR3) | ENSP00000290354.5:p.Asp219= | |
NM_001236.3:c.656A= (CBR3) | NP_001227.1:p.Asp219= | |
NR_038892.1:n.114T= (CBR3-AS1) | ||
NR_038893.1:n.114T= (CBR3-AS1) | ||
NR_038894.1:n.114T= (CBR3-AS1) | ||
NM_001236.4:c.656A= (CBR3) MANE Select | NP_001227.1:p.Asp219= |