Canonical Allele Identifier: CA2719087788
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs2132875691

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140628T>C , CM000671.2:g.21140628T>C GRCh38
NC_000009.11:g.21140627T>C , CM000671.1:g.21140627T>C GRCh37
NC_000009.10:g.21130627T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*355A>G ENSP00000369578.2:n.*355A>G