Canonical Allele Identifier: CA2689577875
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140479-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140479T>A , CM000671.2:g.21140479T>A GRCh38
NC_000009.11:g.21140478T>A , CM000671.1:g.21140478T>A GRCh37
NC_000009.10:g.21130478T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.3:c.*504A>T ENSP00000369578.2:n.*504A>T
Search 100 bp 5'
Search 100 bp 3'