Canonical Allele Identifier: CA2689577892
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140570-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140570A>G , CM000671.2:g.21140570A>G GRCh38
NC_000009.11:g.21140569A>G , CM000671.1:g.21140569A>G GRCh37
NC_000009.10:g.21130569A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*413T>C ENSP00000369578.2:n.*413T>C