Canonical Allele Identifier: CA862082714
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs1484433348
gnomAD v3: 9-21140644-T-A
gnomAD v4: 9-21140644-T-A
MyVariant Identifiers: chr9:g.21140643T>A (hg19) chr9:g.21140644T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140644T>A , CM000671.2:g.21140644T>A GRCh38
NC_000009.11:g.21140643T>A , CM000671.1:g.21140643T>A GRCh37
NC_000009.10:g.21130643T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.4:c.*339A>T MANE Select ENSP00000369578.2:n.*339A>T
ENST00000380229.3:c.*339A>T ENSP00000369578.2:n.*339A>T
NM_002177.1:c.*339A>T NP_002168.1:n.*339A>T
NM_002177.2:c.*339A>T NP_002168.1:n.*339A>T
NM_002177.3:c.*339A>T MANE Select NP_002168.1:n.*339A>T
Search 100 bp 5'
Search 100 bp 3'