Canonical Allele Identifier: CA2689577881
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140510-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140510A>T , CM000671.2:g.21140510A>T GRCh38
NC_000009.11:g.21140509A>T , CM000671.1:g.21140509A>T GRCh37
NC_000009.10:g.21130509A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*473T>A ENSP00000369578.2:n.*473T>A