Canonical Allele Identifier: CA862082675

Gene: IFNW1

Linked Data

• dbSNP Id: rs1325723840
• MyVariant Identifiers: chr9:g.21140481C>T (hg19) ; chr9:g.21140482C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21140482C>T , CM000671.2:g.21140482C>T	GRCh38
NC_000009.11:g.21140481C>T , CM000671.1:g.21140481C>T	GRCh37
NC_000009.10:g.21130481C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000380229.3:c.*501G>A	ENSP00000369578.2:n.*501G>A