Canonical Allele Identifier: CA378891054
Gene: IFITM5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.299436C>G (hg19) chr11:g.299436C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299436C>G , CM000673.2:g.299436C>G GRCh38
NC_000011.9:g.299436C>G , CM000673.1:g.299436C>G GRCh37
NC_000011.8:g.289436C>G NCBI36
NG_032892.1:g.5091G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.55G>C MANE Select ENSP00000372059.2:p.Gly19Arg
NM_001025295.2:c.55G>C NP_001020466.1:p.Gly19Arg
NM_001025295.3:c.55G>C MANE Select NP_001020466.1:p.Gly19Arg
Search 100 bp 5'
Search 100 bp 3'