Canonical Allele Identifier: CA1838717585
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs1249267636

Genomic Alleles

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

Transcript Alleles

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