Canonical Allele Identifier: CA378891039

Gene: IFITM5

Linked Data

• MyVariant Identifiers: chr11:g.299430G>C (hg19) ; chr11:g.299430G>C (hg38)

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