Canonical Allele Identifier: CA5773518

Gene: IFITM5

Linked Data

• dbSNP Id: rs778848693
• ExAC: 11:299427 T / C
• gnomAD v2: 11-299427-T-C
• gnomAD v4: 11-299427-T-C
• MyVariant Identifiers: chr11:g.299427T>C (hg19) ; chr11:g.299427T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299427T>C , CM000673.2:g.299427T>C	GRCh38
NC_000011.9:g.299427T>C , CM000673.1:g.299427T>C	GRCh37
NC_000011.8:g.289427T>C	NCBI36
NG_032892.1:g.5100A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.64A>G MANE Select	ENSP00000372059.2:p.Thr22Ala
NM_001025295.2:c.64A>G	NP_001020466.1:p.Thr22Ala
NM_001025295.3:c.64A>G MANE Select	NP_001020466.1:p.Thr22Ala