Canonical Allele Identifier: CA2689577963
Gene: IFNW1 HGNC NCBI

Linked Data

gnomAD v4: 9-21140710-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140710C>A , CM000671.2:g.21140710C>A GRCh38
NC_000009.11:g.21140709C>A , CM000671.1:g.21140709C>A GRCh37
NC_000009.10:g.21130709C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.4:c.*273G>T MANE Select ENSP00000369578.2:n.*273G>T
ENST00000380229.3:c.*273G>T ENSP00000369578.2:n.*273G>T
NM_002177.1:c.*273G>T NP_002168.1:n.*273G>T
NM_002177.2:c.*273G>T NP_002168.1:n.*273G>T
NM_002177.3:c.*273G>T MANE Select NP_002168.1:n.*273G>T
Search 100 bp 5'
Search 100 bp 3'