Canonical Allele Identifier: CA597017741

Gene: IFITM5

Linked Data

• dbSNP Id: rs1202397723
• gnomAD v2: 11-299434-AC-A
• gnomAD v4: 11-299434-AC-A
• MyVariant Identifiers: chr11:g.299435del (hg19) ; chr11:g.299435del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299436del , CM000673.2:g.299436del	GRCh38
NC_000011.9:g.299436del , CM000673.1:g.299436del	GRCh37
NC_000011.8:g.289436del	NCBI36
NG_032892.1:g.5092del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.56del MANE Select	ENSP00000372059.2:p.Gly19ValfsTer19
NM_001025295.2:c.56del	NP_001020466.1:p.Gly19ValfsTer19
NM_001025295.3:c.56del MANE Select	NP_001020466.1:p.Gly19ValfsTer19