Canonical Allele Identifier: CA190627598
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs368762176
gnomAD v3: 9-21140558-G-C
gnomAD v4: 9-21140558-G-C
MyVariant Identifiers: chr9:g.21140557G>C (hg19) chr9:g.21140558G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140558G>C , CM000671.2:g.21140558G>C GRCh38
NC_000009.11:g.21140557G>C , CM000671.1:g.21140557G>C GRCh37
NC_000009.10:g.21130557G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*425C>G ENSP00000369578.2:n.*425C>G
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