Canonical Allele Identifier: CA378890877
Gene: IFITM5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299387T>A , CM000673.2:g.299387T>A GRCh38
NC_000011.9:g.299387T>A , CM000673.1:g.299387T>A GRCh37
NC_000011.8:g.289387T>A NCBI36
NG_032892.1:g.5140A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.104A>T MANE Select ENSP00000372059.2:p.Asp35Val
NM_001025295.2:c.104A>T NP_001020466.1:p.Asp35Val
NM_001025295.3:c.104A>T MANE Select NP_001020466.1:p.Asp35Val