Canonical Allele Identifier: CA1947011651
Gene: IFITM5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299469C= , CM000673.2:g.299469C= GRCh38
NC_000011.9:g.299469C= , CM000673.1:g.299469C= GRCh37
NC_000011.8:g.289469C= NCBI36
NG_032892.1:g.5058G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.22G= MANE Select ENSP00000372059.2:p.Glu8=
NM_001025295.2:c.22G= NP_001020466.1:p.Glu8=
NM_001025295.3:c.22G= MANE Select NP_001020466.1:p.Glu8=
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