Canonical Allele Identifier: CA2689577901
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140642-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140642A>G , CM000671.2:g.21140642A>G GRCh38
NC_000009.11:g.21140641A>G , CM000671.1:g.21140641A>G GRCh37
NC_000009.10:g.21130641A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.4:c.*341T>C MANE Select ENSP00000369578.2:n.*341T>C
ENST00000380229.3:c.*341T>C ENSP00000369578.2:n.*341T>C
NM_002177.1:c.*341T>C NP_002168.1:n.*341T>C
NM_002177.2:c.*341T>C NP_002168.1:n.*341T>C
NM_002177.3:c.*341T>C MANE Select NP_002168.1:n.*341T>C