Canonical Allele Identifier: CA190627618

Gene: IFNW1

Linked Data

• dbSNP Id: rs911083835
• gnomAD v4: 9-21140594-G-A
• MyVariant Identifiers: chr9:g.21140593G>A (hg19) ; chr9:g.21140594G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21140594G>A , CM000671.2:g.21140594G>A	GRCh38
NC_000009.11:g.21140593G>A , CM000671.1:g.21140593G>A	GRCh37
NC_000009.10:g.21130593G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380229.3:c.*389C>T	ENSP00000369578.2:n.*389C>T