Canonical Allele Identifier: CA378890804
Gene: IFITM5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.299366A>T (hg19) chr11:g.299366A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299366A>T , CM000673.2:g.299366A>T GRCh38
NC_000011.9:g.299366A>T , CM000673.1:g.299366A>T GRCh37
NC_000011.8:g.289366A>T NCBI36
NG_032892.1:g.5161T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.125T>A MANE Select ENSP00000372059.2:p.Phe42Tyr
NM_001025295.2:c.125T>A NP_001020466.1:p.Phe42Tyr
NM_001025295.3:c.125T>A MANE Select NP_001020466.1:p.Phe42Tyr
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