Canonical Allele Identifier: CA2783169921
Gene: IFNW1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140605T>C , CM000671.2:g.21140605T>C GRCh38
NC_000009.11:g.21140604T>C , CM000671.1:g.21140604T>C GRCh37
NC_000009.10:g.21130604T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*378A>G ENSP00000369578.2:n.*378A>G