Canonical Allele Identifier: CA862082730
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs1175142119
gnomAD v3: 9-21140719-G-T
gnomAD v4: 9-21140719-G-T
MyVariant Identifiers: chr9:g.21140718G>T (hg19) chr9:g.21140719G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140719G>T , CM000671.2:g.21140719G>T GRCh38
NC_000009.11:g.21140718G>T , CM000671.1:g.21140718G>T GRCh37
NC_000009.10:g.21130718G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380229.4:c.*264C>A MANE Select ENSP00000369578.2:n.*264C>A
ENST00000380229.3:c.*264C>A ENSP00000369578.2:n.*264C>A
NM_002177.1:c.*264C>A NP_002168.1:n.*264C>A
NM_002177.2:c.*264C>A NP_002168.1:n.*264C>A
NM_002177.3:c.*264C>A MANE Select NP_002168.1:n.*264C>A
Search 100 bp 5'
Search 100 bp 3'