Canonical Allele Identifier: CA862082687

Gene: IFNW1

Linked Data

• dbSNP Id: rs1249267636
• gnomAD v3: 9-21140514-A-G
• gnomAD v4: 9-21140514-A-G
• MyVariant Identifiers: chr9:g.21140513A>G (hg19) ; chr9:g.21140514A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21140514A>G , CM000671.2:g.21140514A>G	GRCh38
NC_000009.11:g.21140513A>G , CM000671.1:g.21140513A>G	GRCh37
NC_000009.10:g.21130513A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380229.3:c.*469T>C	ENSP00000369578.2:n.*469T>C