Canonical Allele Identifier: CA2719087831
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs2132875735
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140700T>A , CM000671.2:g.21140700T>A GRCh38
NC_000009.11:g.21140699T>A , CM000671.1:g.21140699T>A GRCh37
NC_000009.10:g.21130699T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.4:c.*283A>T MANE Select ENSP00000369578.2:n.*283A>T
ENST00000380229.3:c.*283A>T ENSP00000369578.2:n.*283A>T
NM_002177.1:c.*283A>T NP_002168.1:n.*283A>T
NM_002177.2:c.*283A>T NP_002168.1:n.*283A>T
NM_002177.3:c.*283A>T MANE Select NP_002168.1:n.*283A>T
Search 100 bp 5'
Search 100 bp 3'