Canonical Allele Identifier: CA586867859
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs1276271249
gnomAD v2: 9-21140727-T-G
gnomAD v3: 9-21140728-T-G
gnomAD v4: 9-21140728-T-G
MyVariant Identifiers: chr9:g.21140727T>G (hg19) chr9:g.21140728T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140728T>G , CM000671.2:g.21140728T>G GRCh38
NC_000009.11:g.21140727T>G , CM000671.1:g.21140727T>G GRCh37
NC_000009.10:g.21130727T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.4:c.*255A>C MANE Select ENSP00000369578.2:n.*255A>C
ENST00000380229.3:c.*255A>C ENSP00000369578.2:n.*255A>C
NM_002177.1:c.*255A>C NP_002168.1:n.*255A>C
NM_002177.2:c.*255A>C NP_002168.1:n.*255A>C
NM_002177.3:c.*255A>C MANE Select NP_002168.1:n.*255A>C
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