Canonical Allele Identifier: CA5773505

Gene: IFITM5

Linked Data

• dbSNP Id: rs776961228
• ExAC: 11:299406 G / A
• gnomAD v2: 11-299406-G-A
• gnomAD v4: 11-299406-G-A
• MyVariant Identifiers: chr11:g.299406G>A (hg19) ; chr11:g.299406G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299406G>A , CM000673.2:g.299406G>A	GRCh38
NC_000011.9:g.299406G>A , CM000673.1:g.299406G>A	GRCh37
NC_000011.8:g.289406G>A	NCBI36
NG_032892.1:g.5121C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.85C>T MANE Select	ENSP00000372059.2:p.Pro29Ser
NM_001025295.2:c.85C>T	NP_001020466.1:p.Pro29Ser
NM_001025295.3:c.85C>T MANE Select	NP_001020466.1:p.Pro29Ser