Canonical Allele Identifier: CA216904611

Gene: IFITM5

Linked Data

• dbSNP Id: rs762079301
• gnomAD v4: 11-299459-C-A
• MyVariant Identifiers: chr11:g.299459C>A (hg19) ; chr11:g.299459C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299459C>A , CM000673.2:g.299459C>A	GRCh38
NC_000011.9:g.299459C>A , CM000673.1:g.299459C>A	GRCh37
NC_000011.8:g.289459C>A	NCBI36
NG_032892.1:g.5068G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.32G>T MANE Select	ENSP00000372059.2:p.Arg11Leu
NM_001025295.2:c.32G>T	NP_001020466.1:p.Arg11Leu
NM_001025295.3:c.32G>T MANE Select	NP_001020466.1:p.Arg11Leu