Canonical Allele Identifier: CA308189025

Gene: IFNL4

Linked Data

• dbSNP Id: rs533259477
• gnomAD v2: 19-39738130-A-C
• gnomAD v3: 19-39247490-A-C
• gnomAD v4: 19-39247490-A-C
• MyVariant Identifiers: chr19:g.39738130A>C (hg19) ; chr19:g.39247490A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247490A>C , CM000681.2:g.39247490A>C	GRCh38
NC_000019.9:g.39738130A>C , CM000681.1:g.39738130A>C	GRCh37
NC_000019.8:g.44429970A>C	NCBI36
NG_042193.1:g.2482T>G
NG_055295.1:g.6367T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-27T>G	ENSP00000476098.1:n.368-27T>G
ENST00000610963.1:c.367-27T>G	ENSP00000481371.1:n.367-27T>G
ENST00000616270.4:c.400T>G	ENSP00000480679.1:p.Ser134Ala
ENST00000634680.1:c.152-27T>G	ENSP00000489240.1:n.152-27T>G
ENST00000634967.1:c.224-27T>G	ENSP00000489559.1:n.224-27T>G
NR_074079.1:n.645-27T>G