Canonical Allele Identifier: CA378890828
Gene: IFITM5 HGNC NCBI

Linked Data

dbSNP Id: rs1443010416
gnomAD v2: 11-299375-C-A
gnomAD v3: 11-299375-C-A
gnomAD v4: 11-299375-C-A
MyVariant Identifiers: chr11:g.299375C>A (hg19) chr11:g.299375C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299375C>A , CM000673.2:g.299375C>A GRCh38
NC_000011.9:g.299375C>A , CM000673.1:g.299375C>A GRCh37
NC_000011.8:g.289375C>A NCBI36
NG_032892.1:g.5152G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.116G>T MANE Select ENSP00000372059.2:p.Trp39Leu
NM_001025295.2:c.116G>T NP_001020466.1:p.Trp39Leu
NM_001025295.3:c.116G>T MANE Select NP_001020466.1:p.Trp39Leu
Search 100 bp 5'
Search 100 bp 3'