Canonical Allele Identifier: CA862082677

Gene: IFNW1

Linked Data

• dbSNP Id: rs1458677781
• gnomAD v3: 9-21140498-G-A
• gnomAD v4: 9-21140498-G-A
• MyVariant Identifiers: chr9:g.21140497G>A (hg19) ; chr9:g.21140498G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21140498G>A , CM000671.2:g.21140498G>A	GRCh38
NC_000009.11:g.21140497G>A , CM000671.1:g.21140497G>A	GRCh37
NC_000009.10:g.21130497G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380229.3:c.*485C>T	ENSP00000369578.2:n.*485C>T