Canonical Allele Identifier: CA586867857
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs1344429900
gnomAD v2: 9-21140715-A-T
gnomAD v3: 9-21140716-A-T
gnomAD v4: 9-21140716-A-T
MyVariant Identifiers: chr9:g.21140715A>T (hg19) chr9:g.21140716A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140716A>T , CM000671.2:g.21140716A>T GRCh38
NC_000009.11:g.21140715A>T , CM000671.1:g.21140715A>T GRCh37
NC_000009.10:g.21130715A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.4:c.*267T>A MANE Select ENSP00000369578.2:n.*267T>A
ENST00000380229.3:c.*267T>A ENSP00000369578.2:n.*267T>A
NM_002177.1:c.*267T>A NP_002168.1:n.*267T>A
NM_002177.2:c.*267T>A NP_002168.1:n.*267T>A
NM_002177.3:c.*267T>A MANE Select NP_002168.1:n.*267T>A
Search 100 bp 5'
Search 100 bp 3'