Canonical Allele Identifier: CA378891049
Gene: IFITM5 HGNC NCBI

Linked Data

gnomAD v4: 11-299435-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299435C>A , CM000673.2:g.299435C>A GRCh38
NC_000011.9:g.299435C>A , CM000673.1:g.299435C>A GRCh37
NC_000011.8:g.289435C>A NCBI36
NG_032892.1:g.5092G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.56G>T MANE Select ENSP00000372059.2:p.Gly19Val
NM_001025295.2:c.56G>T NP_001020466.1:p.Gly19Val
NM_001025295.3:c.56G>T MANE Select NP_001020466.1:p.Gly19Val