Canonical Allele Identifier: CA378890742
Gene: IFITM5 HGNC NCBI

Linked Data

dbSNP Id: rs1313835435
gnomAD v2: 11-299352-G-C
MyVariant Identifiers: chr11:g.299352G>C (hg19) chr11:g.299352G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299352G>C , CM000673.2:g.299352G>C GRCh38
NC_000011.9:g.299352G>C , CM000673.1:g.299352G>C GRCh37
NC_000011.8:g.289352G>C NCBI36
NG_032892.1:g.5175C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.139C>G MANE Select ENSP00000372059.2:p.Leu47Val
NM_001025295.2:c.139C>G NP_001020466.1:p.Leu47Val
NM_001025295.3:c.139C>G MANE Select NP_001020466.1:p.Leu47Val
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