Canonical Allele Identifier: CA378891059

Gene: IFITM5

Linked Data

• dbSNP Id: rs1190842682
• gnomAD v3: 11-299438-G-C
• gnomAD v4: 11-299438-G-C
• MyVariant Identifiers: chr11:g.299438G>C (hg19) ; chr11:g.299438G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299438G>C , CM000673.2:g.299438G>C	GRCh38
NC_000011.9:g.299438G>C , CM000673.1:g.299438G>C	GRCh37
NC_000011.8:g.289438G>C	NCBI36
NG_032892.1:g.5089C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.53C>G MANE Select	ENSP00000372059.2:p.Ala18Gly
NM_001025295.2:c.53C>G	NP_001020466.1:p.Ala18Gly
NM_001025295.3:c.53C>G MANE Select	NP_001020466.1:p.Ala18Gly