Canonical Allele Identifier: CA10237281
Gene: APOBEC3B HGNC NCBI
APOBEC3A HGNC NCBI
ClinVar RCV:
RCV004076580
ClinVar Variation:
2208143
dbSNP:
372003442
gnomAD v2:
22:39380157 A / G
gnomAD v3:
22:38984152 A / G
gnomAD v4:
chr22-38984152-A-G
Joint Max Group AF 0.00017801 (AFR)
Genomes Max Group AF 0.00018694 (AFR)
Exomes Max Group AF 0.00009782 (AFR)
MyVariant.info:
GRCh38 chr22:g.38984152A>G
GRCh37 chr22:g.39380157A>G
Revel Score:
ENST00000407298 0.154
ENST00000402182 0.154
ENST00000333467 (MANE Select) 0.154
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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
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