Canonical Allele Identifier: CA13408114
Gene: TRIM5 HGNC NCBI

Linked Data

dbSNP Id: rs3858526
gnomAD v2: 11-5959757-A-C
gnomAD v3: 11-5938527-A-C
gnomAD v4: 11-5938527-A-C
MyVariant Identifiers: chr11:g.5959757A>C (hg19) chr11:g.5938527A>C (hg38)
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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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