Canonical Allele Identifier: CA1838717581

Gene: IFNW1

Linked Data

• dbSNP Id: rs1312218475
• gnomAD v3: 9-21140512-A-C
• gnomAD v4: 9-21140512-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21140512A>C , CM000671.2:g.21140512A>C	GRCh38
NC_000009.11:g.21140511A>C , CM000671.1:g.21140511A>C	GRCh37
NC_000009.10:g.21130511A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380229.3:c.*471T>G	ENSP00000369578.2:n.*471T>G