ClinVar RCV:
ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.38984152A>G , CM000684.2:g.38984152A>G | GRCh38 |
| NC_000022.10:g.39380157A>G , CM000684.1:g.39380157A>G | GRCh37 |
| NC_000022.9:g.37710103A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333467.4:c.95A>G (APOBEC3B) MANE Select | ENSP00000327459.3:p.Tyr32Cys | |
| ENST00000333467.3:c.95A>G (APOBEC3B) | ENSP00000327459.3:p.Tyr32Cys | |
| ENST00000335760.9:c.95A>G (APOBEC3B) | ENSP00000338897.5:p.Tyr32Cys | |
| ENST00000402182.7:c.95A>G (APOBEC3B) | ENSP00000385060.3:p.Tyr32Cys | |
| ENST00000407298.7:c.95A>G (APOBEC3B) | ENSP00000385068.3:p.Tyr32Cys | |
| ENST00000618553.1:c.586-8279A>G (APOBEC3A) | ENSP00000481904.1:n.586-8279A>G | |
| NM_001270411.1:c.95A>G (APOBEC3B) | NP_001257340.1:p.Tyr32Cys | |
| NM_004900.4:c.95A>G (APOBEC3B) | NP_004891.4:p.Tyr32Cys | |
| NM_004900.5:c.95A>G (APOBEC3B) MANE Select | NP_004891.5:p.Tyr32Cys | |
| NM_001270411.2:c.95A>G (APOBEC3B) | NP_001257340.2:p.Tyr32Cys |