Canonical Allele Identifier: CA378891061
Gene: IFITM5 HGNC NCBI

Linked Data

gnomAD v4: 11-299438-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299438G>T , CM000673.2:g.299438G>T GRCh38
NC_000011.9:g.299438G>T , CM000673.1:g.299438G>T GRCh37
NC_000011.8:g.289438G>T NCBI36
NG_032892.1:g.5089C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.53C>A MANE Select ENSP00000372059.2:p.Ala18Asp
NM_001025295.2:c.53C>A NP_001020466.1:p.Ala18Asp
NM_001025295.3:c.53C>A MANE Select NP_001020466.1:p.Ala18Asp