Canonical Allele Identifier: CA2689577878
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140503-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140503T>C , CM000671.2:g.21140503T>C GRCh38
NC_000009.11:g.21140502T>C , CM000671.1:g.21140502T>C GRCh37
NC_000009.10:g.21130502T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*480A>G ENSP00000369578.2:n.*480A>G
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