Canonical Allele Identifier: CA2689577874
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140475-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140475T>C , CM000671.2:g.21140475T>C GRCh38
NC_000009.11:g.21140474T>C , CM000671.1:g.21140474T>C GRCh37
NC_000009.10:g.21130474T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.3:c.*508A>G ENSP00000369578.2:n.*508A>G
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