Canonical Allele Identifier: CA1838717590
Gene: IFNW1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140527G= , CM000671.2:g.21140527G= GRCh38
NC_000009.11:g.21140526G= , CM000671.1:g.21140526G= GRCh37
NC_000009.10:g.21130526G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*456C= ENSP00000369578.2:n.*456C=