Canonical Allele Identifier: CA472303480

Gene: IFITM5

Linked Data

• dbSNP Id: rs587776916
• gnomAD v2: 11-299504-G-C
• gnomAD v4: 11-299504-G-C
• MyVariant Identifiers: chr11:g.299504G>C (hg19) ; chr11:g.299504G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299504G>C , CM000673.2:g.299504G>C	GRCh38
NC_000011.9:g.299504G>C , CM000673.1:g.299504G>C	GRCh37
NC_000011.8:g.289504G>C	NCBI36
NG_032892.1:g.5023C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.-14C>G MANE Select	ENSP00000372059.2:n.-14C>G
NM_001025295.2:c.-14C>G	NP_001020466.1:n.-14C>G
NM_001025295.3:c.-14C>G MANE Select	NP_001020466.1:n.-14C>G