Canonical Allele Identifier: CA5773538

Gene: IFITM5

Linked Data

• dbSNP Id: rs777569246
• ExAC: 11:299489 A / T
• gnomAD v2: 11-299489-A-T
• gnomAD v3: 11-299489-A-T
• gnomAD v4: 11-299489-A-T
• MyVariant Identifiers: chr11:g.299489A>T (hg19) ; chr11:g.299489A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299489A>T , CM000673.2:g.299489A>T	GRCh38
NC_000011.9:g.299489A>T , CM000673.1:g.299489A>T	GRCh37
NC_000011.8:g.289489A>T	NCBI36
NG_032892.1:g.5038T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.2T>A MANE Select	ENSP00000372059.2:p.Met1Lys
NM_001025295.2:c.2T>A	NP_001020466.1:p.Met1Lys
NM_001025295.3:c.2T>A MANE Select	NP_001020466.1:p.Met1Lys