Canonical Allele Identifier: CA5773489
Gene: IFITM5 HGNC NCBI

Linked Data

dbSNP Id: rs138776304
ExAC: 11:299390 C / G
gnomAD v2: 11-299390-C-G
MyVariant Identifiers: chr11:g.299390C>G (hg19) chr11:g.299390C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299390C>G , CM000673.2:g.299390C>G GRCh38
NC_000011.9:g.299390C>G , CM000673.1:g.299390C>G GRCh37
NC_000011.8:g.289390C>G NCBI36
NG_032892.1:g.5137G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.101G>C MANE Select ENSP00000372059.2:p.Arg34Pro
NM_001025295.2:c.101G>C NP_001020466.1:p.Arg34Pro
NM_001025295.3:c.101G>C MANE Select NP_001020466.1:p.Arg34Pro
Search 100 bp 5'
Search 100 bp 3'