Canonical Allele Identifier: CA216904687
Gene: IFITM5 HGNC NCBI

Linked Data

dbSNP Id: rs866030579
gnomAD v4: 11-299488-C-T
MyVariant Identifiers: chr11:g.299488C>T (hg19) chr11:g.299488C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299488C>T , CM000673.2:g.299488C>T GRCh38
NC_000011.9:g.299488C>T , CM000673.1:g.299488C>T GRCh37
NC_000011.8:g.289488C>T NCBI36
NG_032892.1:g.5039G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.3G>A MANE Select ENSP00000372059.2:p.Met1Ile
NM_001025295.2:c.3G>A NP_001020466.1:p.Met1Ile
NM_001025295.3:c.3G>A MANE Select NP_001020466.1:p.Met1Ile
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