Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118894891A= , CM000673.2:g.118894891A= | GRCh38 |
| NC_000011.9:g.118765600A= , CM000673.1:g.118765600A= | GRCh37 |
| NC_000011.8:g.118270810A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000292174.5:c.*228A= (CXCR5) MANE Select | ENSP00000292174.4:n.*228A= | |
| ENST00000292174.4:c.*228A= (CXCR5) | ENSP00000292174.4:n.*228A= | |
| ENST00000334801.7:c.*3524T= (BCL9L) | ENSP00000335320.3:n.*3524T= | |
| NM_001716.4:c.*228A= (CXCR5) | NP_001707.1:n.*228A= | |
| NM_032966.2:c.*228A= (CXCR5) | NP_116743.1:n.*228A= | |
| NM_001716.5:c.*228A= (CXCR5) MANE Select | NP_001707.1:n.*228A= | |
| NM_182557.3:c.*3524T= (BCL9L) | NP_872363.1:n.*3524T= |