Canonical Allele Identifier: CA5773502
Gene: IFITM5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1647822
ClinVar RCV Id: RCV002139294
dbSNP Id: rs201497459
ExAC: 11:299405 G / A
gnomAD v2: 11-299405-G-A
gnomAD v3: 11-299405-G-A
gnomAD v4: 11-299405-G-A
COSMIC: COSM1353370
MyVariant Identifiers: chr11:g.299405G>A (hg19) chr11:g.299405G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.299405G>A , CM000673.2:g.299405G>A GRCh38
NC_000011.9:g.299405G>A , CM000673.1:g.299405G>A GRCh37
NC_000011.8:g.289405G>A NCBI36
NG_032892.1:g.5122C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382614.2:c.86C>T MANE Select ENSP00000372059.2:p.Pro29Leu
NM_001025295.2:c.86C>T NP_001020466.1:p.Pro29Leu
NM_001025295.3:c.86C>T MANE Select NP_001020466.1:p.Pro29Leu
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