Canonical Allele Identifier: CA1838717564
Gene: IFNW1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140501A= , CM000671.2:g.21140501A= GRCh38
NC_000009.11:g.21140500A= , CM000671.1:g.21140500A= GRCh37
NC_000009.10:g.21130500A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*482T= ENSP00000369578.2:n.*482T=