Canonical Allele Identifier: CA378891167

Gene: IFITM5

Linked Data

• dbSNP Id: rs1329429081
• gnomAD v2: 11-299466-C-T
• gnomAD v4: 11-299466-C-T
• COSMIC: COSM5717547
• MyVariant Identifiers: chr11:g.299466C>T (hg19) ; chr11:g.299466C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299466C>T , CM000673.2:g.299466C>T	GRCh38
NC_000011.9:g.299466C>T , CM000673.1:g.299466C>T	GRCh37
NC_000011.8:g.289466C>T	NCBI36
NG_032892.1:g.5061G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.25G>A MANE Select	ENSP00000372059.2:p.Asp9Asn
NM_001025295.2:c.25G>A	NP_001020466.1:p.Asp9Asn
NM_001025295.3:c.25G>A MANE Select	NP_001020466.1:p.Asp9Asn