Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.36135469G= , CM000683.2:g.36135469G= | GRCh38 |
| NC_000021.8:g.37507767G= , CM000683.1:g.37507767G= | GRCh37 |
| NC_000021.7:g.36429637G= | NCBI36 |
| NG_052818.1:g.5569G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001236.4:c.277G= (CBR3) MANE Select | NP_001227.1:p.Val93= |
| ENST00000290354.6:c.277G= (CBR3) MANE Select | ENSP00000290354.5:p.Val93= |
| NM_001236.3:c.277G= (CBR3) | NP_001227.1:p.Val93= |
| NR_038892.1:n.193-1708C= (CBR3-AS1) | |
| NR_038893.1:n.193-2395C= (CBR3-AS1) | |
| ENST00000290354.5:c.277G= (CBR3) | ENSP00000290354.5:p.Val93= |
| XM_011529772.1:c.277G= (CBR3) | XP_011528074.1:p.Val93= |
| XM_011529772.2:c.277G= (CBR3) | XP_011528074.1:p.Val93= |