Canonical Allele Identifier: CA586867853
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs1361103140
gnomAD v2: 9-21140706-A-G
gnomAD v3: 9-21140707-A-G
gnomAD v4: 9-21140707-A-G
MyVariant Identifiers: chr9:g.21140706A>G (hg19) chr9:g.21140707A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140707A>G , CM000671.2:g.21140707A>G GRCh38
NC_000009.11:g.21140706A>G , CM000671.1:g.21140706A>G GRCh37
NC_000009.10:g.21130706A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.4:c.*276T>C MANE Select ENSP00000369578.2:n.*276T>C
ENST00000380229.3:c.*276T>C ENSP00000369578.2:n.*276T>C
NM_002177.1:c.*276T>C NP_002168.1:n.*276T>C
NM_002177.2:c.*276T>C NP_002168.1:n.*276T>C
NM_002177.3:c.*276T>C MANE Select NP_002168.1:n.*276T>C
Search 100 bp 5'
Search 100 bp 3'