Canonical Allele Identifier: CA2689577900
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140632-GTTTGAAAATAATTTAATAAATAACAAAATACAATATTT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140633_21140670del , CM000671.2:g.21140633_21140670del GRCh38
NC_000009.11:g.21140632_21140669del , CM000671.1:g.21140632_21140669del GRCh37
NC_000009.10:g.21130632_21130669del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.4:c.*313_*350del MANE Select ENSP00000369578.2:n.*313_*350del
ENST00000380229.3:c.*313_*350del ENSP00000369578.2:n.*313_*350del
NM_002177.1:c.*313_*350del NP_002168.1:n.*313_*350del
NM_002177.2:c.*313_*350del NP_002168.1:n.*313_*350del
NM_002177.3:c.*313_*350del MANE Select NP_002168.1:n.*313_*350del
Search 100 bp 5'
Search 100 bp 3'