Canonical Allele Identifier: CA1838717598
Gene: IFNW1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140529A= , CM000671.2:g.21140529A= GRCh38
NC_000009.11:g.21140528A= , CM000671.1:g.21140528A= GRCh37
NC_000009.10:g.21130528A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*454T= ENSP00000369578.2:n.*454T=