Canonical Allele Identifier: CA1838717554
Gene: IFNW1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140489T= , CM000671.2:g.21140489T= GRCh38
NC_000009.11:g.21140488T= , CM000671.1:g.21140488T= GRCh37
NC_000009.10:g.21130488T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*494A= ENSP00000369578.2:n.*494A=