Canonical Allele Identifier: CA378891039
Gene: IFITM5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299430G>C , CM000673.2:g.299430G>C GRCh38
NC_000011.9:g.299430G>C , CM000673.1:g.299430G>C GRCh37
NC_000011.8:g.289430G>C NCBI36
NG_032892.1:g.5097C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.61C>G MANE Select ENSP00000372059.2:p.His21Asp
NM_001025295.2:c.61C>G NP_001020466.1:p.His21Asp
NM_001025295.3:c.61C>G MANE Select NP_001020466.1:p.His21Asp