Canonical Allele Identifier: CA1122114496
Gene: IFNW1 HGNC NCBI

Linked Data

dbSNP Id: rs1819382137

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21140475_21140476dup , CM000671.2:g.21140475_21140476dup GRCh38
NC_000009.11:g.21140474_21140475dup , CM000671.1:g.21140474_21140475dup GRCh37
NC_000009.10:g.21130474_21130475dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380229.3:c.*507_*508dup ENSP00000369578.2:n.*507_*508dup