Canonical Allele Identifier: CA2689577965
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140714-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140714G>T , CM000671.2:g.21140714G>T GRCh38
NC_000009.11:g.21140713G>T , CM000671.1:g.21140713G>T GRCh37
NC_000009.10:g.21130713G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.4:c.*269C>A MANE Select ENSP00000369578.2:n.*269C>A
ENST00000380229.3:c.*269C>A ENSP00000369578.2:n.*269C>A
NM_002177.1:c.*269C>A NP_002168.1:n.*269C>A
NM_002177.2:c.*269C>A NP_002168.1:n.*269C>A
NM_002177.3:c.*269C>A MANE Select NP_002168.1:n.*269C>A
Search 100 bp 5'
Search 100 bp 3'