Canonical Allele Identifier: CA190627655

Gene: IFNW1

Linked Data

• dbSNP Id: rs139377972
• gnomAD v2: 9-21140678-G-C
• gnomAD v3: 9-21140679-G-C
• gnomAD v4: 9-21140679-G-C
• MyVariant Identifiers: chr9:g.21140678G>C (hg19) ; chr9:g.21140679G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21140679G>C , CM000671.2:g.21140679G>C	GRCh38
NC_000009.11:g.21140678G>C , CM000671.1:g.21140678G>C	GRCh37
NC_000009.10:g.21130678G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000380229.4:c.*304C>G MANE Select	ENSP00000369578.2:n.*304C>G
ENST00000380229.3:c.*304C>G	ENSP00000369578.2:n.*304C>G
NM_002177.1:c.*304C>G	NP_002168.1:n.*304C>G
NM_002177.2:c.*304C>G	NP_002168.1:n.*304C>G
NM_002177.3:c.*304C>G MANE Select	NP_002168.1:n.*304C>G