Canonical Allele Identifier: CA378891123
Gene: IFITM5 HGNC NCBI

Linked Data

gnomAD v4: 11-299453-G-T
MyVariant Identifiers: chr11:g.299453G>T (hg19) chr11:g.299453G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299453G>T , CM000673.2:g.299453G>T GRCh38
NC_000011.9:g.299453G>T , CM000673.1:g.299453G>T GRCh37
NC_000011.8:g.289453G>T NCBI36
NG_032892.1:g.5074C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.38C>A MANE Select ENSP00000372059.2:p.Pro13His
NM_001025295.2:c.38C>A NP_001020466.1:p.Pro13His
NM_001025295.3:c.38C>A MANE Select NP_001020466.1:p.Pro13His
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