Canonical Allele Identifier: CA597017744

Gene: IFITM5

Linked Data

• ClinVar Variation Id: 1273689
• ClinVar RCV Id: RCV002276859 ; RCV001682152
• dbSNP Id: rs1362690516
• gnomAD v2: 11-299493-G-A
• gnomAD v3: 11-299493-G-A
• gnomAD v4: 11-299493-G-A
• MyVariant Identifiers: chr11:g.299493G>A (hg19) ; chr11:g.299493G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299493G>A , CM000673.2:g.299493G>A	GRCh38
NC_000011.9:g.299493G>A , CM000673.1:g.299493G>A	GRCh37
NC_000011.8:g.289493G>A	NCBI36
NG_032892.1:g.5034C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.-3C>T MANE Select	ENSP00000372059.2:n.-3C>T
NM_001025295.2:c.-3C>T	NP_001020466.1:n.-3C>T
NM_001025295.3:c.-3C>T MANE Select	NP_001020466.1:n.-3C>T