Canonical Allele Identifier: CA5773513

Gene: IFITM5

Linked Data

• dbSNP Id: rs755605446
• ExAC: 11:299418 T / C
• gnomAD v2: 11-299418-T-C
• gnomAD v4: 11-299418-T-C
• MyVariant Identifiers: chr11:g.299418T>C (hg19) ; chr11:g.299418T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.299418T>C , CM000673.2:g.299418T>C	GRCh38
NC_000011.9:g.299418T>C , CM000673.1:g.299418T>C	GRCh37
NC_000011.8:g.289418T>C	NCBI36
NG_032892.1:g.5109A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382614.2:c.73A>G MANE Select	ENSP00000372059.2:p.Thr25Ala
NM_001025295.2:c.73A>G	NP_001020466.1:p.Thr25Ala
NM_001025295.3:c.73A>G MANE Select	NP_001020466.1:p.Thr25Ala