Canonical Allele Identifier: CA2689577891
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140566-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140566C>T , CM000671.2:g.21140566C>T GRCh38
NC_000009.11:g.21140565C>T , CM000671.1:g.21140565C>T GRCh37
NC_000009.10:g.21130565C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*417G>A ENSP00000369578.2:n.*417G>A