Canonical Allele Identifier: CA862082688
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs1191027136
MyVariant Identifiers: chr9:g.21140523A>G (hg19) chr9:g.21140524A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140524A>G , CM000671.2:g.21140524A>G GRCh38
NC_000009.11:g.21140523A>G , CM000671.1:g.21140523A>G GRCh37
NC_000009.10:g.21130523A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*459T>C ENSP00000369578.2:n.*459T>C
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