HGVS | Genome Assembly |
---|---|
NC_000021.9:g.36140129T= , CM000683.2:g.36140129T= | GRCh38 |
NC_000021.8:g.37512427T= , CM000683.1:g.37512427T= | GRCh37 |
NC_000021.7:g.36434297T= | NCBI36 |
NG_052818.1:g.10229T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000290354.6:c.397+2197T= (CBR3) MANE Select | ENSP00000290354.5:n.397+2197T= | |
ENST00000290354.5:c.397+2197T= (CBR3) | ENSP00000290354.5:n.397+2197T= | |
NM_001236.3:c.397+2197T= (CBR3) | NP_001227.1:n.397+2197T= | |
NR_038892.1:n.192+6127A= (CBR3-AS1) | ||
NR_038893.1:n.192+6127A= (CBR3-AS1) | ||
XM_011529772.1:c.398-1795T= (CBR3) | XP_011528074.1:n.398-1795T= | |
XM_011529772.2:c.398-1795T= (CBR3) | XP_011528074.1:n.398-1795T= | |
NM_001236.4:c.397+2197T= (CBR3) MANE Select | NP_001227.1:n.397+2197T= |