Canonical Allele Identifier: CA5773482
Gene: IFITM5 HGNC NCBI

Linked Data

dbSNP Id: rs753826000
ExAC: 11:299370 C / T
gnomAD v2: 11-299370-C-T
gnomAD v3: 11-299370-C-T
gnomAD v4: 11-299370-C-T
COSMIC: COSM5623321
MyVariant Identifiers: chr11:g.299370C>T (hg19) chr11:g.299370C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299370C>T , CM000673.2:g.299370C>T GRCh38
NC_000011.9:g.299370C>T , CM000673.1:g.299370C>T GRCh37
NC_000011.8:g.289370C>T NCBI36
NG_032892.1:g.5157G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.121G>A MANE Select ENSP00000372059.2:p.Val41Met
NM_001025295.2:c.121G>A NP_001020466.1:p.Val41Met
NM_001025295.3:c.121G>A MANE Select NP_001020466.1:p.Val41Met
Search 100 bp 5'
Search 100 bp 3'