Canonical Allele Identifier: CA378891231

Gene: IFITM5

Linked Data

• dbSNP Id: rs376963969
• gnomAD v3: 11-299483-G-T
• gnomAD v4: 11-299483-G-T
• MyVariant Identifiers: chr11:g.299483G>T (hg19) ; chr11:g.299483G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299483G>T , CM000673.2:g.299483G>T	GRCh38
NC_000011.9:g.299483G>T , CM000673.1:g.299483G>T	GRCh37
NC_000011.8:g.289483G>T	NCBI36
NG_032892.1:g.5044C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.8C>A MANE Select	ENSP00000372059.2:p.Thr3Lys
NM_001025295.2:c.8C>A	NP_001020466.1:p.Thr3Lys
NM_001025295.3:c.8C>A MANE Select	NP_001020466.1:p.Thr3Lys