Canonical Allele Identifier: CA1947011607
Gene: IFITM5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299405G= , CM000673.2:g.299405G= GRCh38
NC_000011.9:g.299405G= , CM000673.1:g.299405G= GRCh37
NC_000011.8:g.289405G= NCBI36
NG_032892.1:g.5122C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.86C= MANE Select ENSP00000372059.2:p.Pro29=
NM_001025295.2:c.86C= NP_001020466.1:p.Pro29=
NM_001025295.3:c.86C= MANE Select NP_001020466.1:p.Pro29=
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