Canonical Allele Identifier: CA378890840
Gene: IFITM5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.299378A>G (hg19) chr11:g.299378A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299378A>G , CM000673.2:g.299378A>G GRCh38
NC_000011.9:g.299378A>G , CM000673.1:g.299378A>G GRCh37
NC_000011.8:g.289378A>G NCBI36
NG_032892.1:g.5149T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.113T>C MANE Select ENSP00000372059.2:p.Ile38Thr
NM_001025295.2:c.113T>C NP_001020466.1:p.Ile38Thr
NM_001025295.3:c.113T>C MANE Select NP_001020466.1:p.Ile38Thr
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Search 100 bp 3'