Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.36135203G>A , CM000683.2:g.36135203G>A | GRCh38 |
| NC_000021.8:g.37507501G>A , CM000683.1:g.37507501G>A | GRCh37 |
| NC_000021.7:g.36429371G>A | NCBI36 |
| NG_052818.1:g.5303G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001236.4:c.11G>A (CBR3) MANE Select | NP_001227.1:p.Cys4Tyr |
| ENST00000290354.6:c.11G>A (CBR3) MANE Select | ENSP00000290354.5:p.Cys4Tyr |
| NM_001236.3:c.11G>A (CBR3) | NP_001227.1:p.Cys4Tyr |
| NR_038892.1:n.193-1442C>T (CBR3-AS1) | |
| NR_038893.1:n.193-2129C>T (CBR3-AS1) | |
| ENST00000290354.5:c.11G>A (CBR3) | ENSP00000290354.5:p.Cys4Tyr |
| XM_011529772.1:c.11G>A (CBR3) | XP_011528074.1:p.Cys4Tyr |
| XM_011529772.2:c.11G>A (CBR3) | XP_011528074.1:p.Cys4Tyr |