Canonical Allele Identifier: CA2689577968
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140728-T-C
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.4:c.*255A>G MANE Select ENSP00000369578.2:n.*255A>G
ENST00000380229.3:c.*255A>G ENSP00000369578.2:n.*255A>G
NM_002177.1:c.*255A>G NP_002168.1:n.*255A>G
NM_002177.2:c.*255A>G NP_002168.1:n.*255A>G
NM_002177.3:c.*255A>G MANE Select NP_002168.1:n.*255A>G
Search 100 bp 5'
Search 100 bp 3'