Canonical Allele Identifier: CA1838717715
Gene: IFNW1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140712A= , CM000671.2:g.21140712A= GRCh38
NC_000009.11:g.21140711A= , CM000671.1:g.21140711A= GRCh37
NC_000009.10:g.21130711A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.4:c.*271T= MANE Select ENSP00000369578.2:n.*271T=
ENST00000380229.3:c.*271T= ENSP00000369578.2:n.*271T=
NM_002177.1:c.*271T= NP_002168.1:n.*271T=
NM_002177.2:c.*271T= NP_002168.1:n.*271T=
NM_002177.3:c.*271T= MANE Select NP_002168.1:n.*271T=
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