Canonical Allele Identifier: CA13408114
Gene: TRIM5 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.5938527A>C
GRCh37 chr11:g.5959757A>C
gnomAD v2:
11:5959757 A / C
gnomAD v3:
11:5938527 A / C
gnomAD v4:
chr11-5938527-A-C
Joint Max Group AF 0.39714676 (AFR)
Genomes Max Group AF 0.39714676 (AFR)
Exomes Max Group AF 0.03553614 (NFE)
dbSNP:
3858526
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5938527A>C , CM000673.2:g.5938527A>C GRCh38
NC_000011.9:g.5959757A>C , CM000673.1:g.5959757A>C GRCh37
NC_000011.8:g.5916333A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000412903.1:c.-334T>G ENSP00000388031.1:n.-334T>G
XR_002957230.1:n.3001T>G
XR_002957231.1:n.288T>G
XR_002957234.1:n.3007T>G
XR_002957235.1:n.3007T>G
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