Canonical Allele Identifier: CA378891119
Gene: IFITM5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.299451T>C (hg19) chr11:g.299451T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299451T>C , CM000673.2:g.299451T>C GRCh38
NC_000011.9:g.299451T>C , CM000673.1:g.299451T>C GRCh37
NC_000011.8:g.289451T>C NCBI36
NG_032892.1:g.5076A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.40A>G MANE Select ENSP00000372059.2:p.Thr14Ala
NM_001025295.2:c.40A>G NP_001020466.1:p.Thr14Ala
NM_001025295.3:c.40A>G MANE Select NP_001020466.1:p.Thr14Ala
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