Canonical Allele Identifier: CA130091
Gene: IFITM5 HGNC NCBI

Linked Data

ClinVar Variation Id: 37143
dbSNP Id: rs587776916
gnomAD v4: 11-299504-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299504G>A , CM000673.2:g.299504G>A GRCh38
NC_000011.9:g.299504G>A , CM000673.1:g.299504G>A GRCh37
NC_000011.8:g.289504G>A NCBI36
NG_032892.1:g.5023C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.-14C>T MANE Select ENSP00000372059.2:n.-14C>T
NM_001025295.2:c.-14C>T NP_001020466.1:n.-14C>T
NM_001025295.3:c.-14C>T MANE Select NP_001020466.1:n.-14C>T