Canonical Allele Identifier: CA5774088
Gene: IFITM3 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.320836C>T
GRCh37 chr11:g.320836C>T
gnomAD v2:
11:320836 C / T
gnomAD v3:
11:320836 C / T
gnomAD v4:
chr11-320836-C-T
Joint Max Group AF 0.49341862 (NFE)
Genomes Max Group AF 0.4827989 (NFE)
Exomes Max Group AF 0.49383838 (NFE)
dbSNP:
34481144
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.320836C>T , CM000673.2:g.320836C>T GRCh38
NC_000011.9:g.320836C>T , CM000673.1:g.320836C>T GRCh37
NC_000011.8:g.310836C>T NCBI36
NG_032755.1:g.5079G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399808.5:c.-23G>A MANE Select ENSP00000382707.4:n.-23G>A
ENST00000531688.2:c.-23G>A ENSP00000473645.2:n.-23G>A
ENST00000679382.1:c.-23G>A ENSP00000505839.1:n.-23G>A
ENST00000679433.1:c.-22-64G>A ENSP00000506209.1:n.-22-64G>A
ENST00000679441.1:c.-22-64G>A ENSP00000506018.1:n.-22-64G>A
ENST00000679792.1:c.-22-64G>A ENSP00000505901.1:n.-22-64G>A
ENST00000680023.1:c.-22-64G>A ENSP00000506536.1:n.-22-64G>A
ENST00000680209.1:c.-23G>A ENSP00000505330.1:n.-23G>A
ENST00000680622.1:c.-22-64G>A ENSP00000505128.1:n.-22-64G>A
ENST00000680720.1:c.-22-64G>A ENSP00000505213.1:n.-22-64G>A
ENST00000680932.1:n.6G>A
ENST00000681184.1:c.-22-64G>A ENSP00000505002.1:n.-22-64G>A
ENST00000681198.1:c.-23G>A ENSP00000506488.1:n.-23G>A
ENST00000681304.1:c.-23G>A ENSP00000506507.1:n.-23G>A
ENST00000681748.1:c.-22-64G>A ENSP00000505936.1:n.-22-64G>A
ENST00000681840.1:c.-23G>A ENSP00000505867.1:n.-23G>A
ENST00000399808.4:c.-23G>A ENSP00000382707.4:n.-23G>A
ENST00000526811.4:c.-22-64G>A ENSP00000432108.1:n.-22-64G>A
ENST00000602735.2:c.-22-64G>A ENSP00000473544.1:n.-22-64G>A
NM_021034.2:c.-23G>A NP_066362.2:n.-23G>A
NR_049759.1:n.79G>A
NM_021034.3:c.-23G>A MANE Select NP_066362.2:n.-23G>A
NR_049759.2:n.25G>A
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