Canonical Allele Identifier: CA1838717713
Gene: IFNW1 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.4:c.*273G= MANE Select ENSP00000369578.2:n.*273G=
ENST00000380229.3:c.*273G= ENSP00000369578.2:n.*273G=
NM_002177.1:c.*273G= NP_002168.1:n.*273G=
NM_002177.2:c.*273G= NP_002168.1:n.*273G=
NM_002177.3:c.*273G= MANE Select NP_002168.1:n.*273G=
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