Canonical Allele Identifier: CA507655560

Gene: IFNL4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247226C>A , CM000681.2:g.39247226C>A	GRCh38
NC_000019.9:g.39737866C>A , CM000681.1:g.39737866C>A	GRCh37
NC_000019.8:g.44429706C>A	NCBI36
NG_042193.1:g.2746G>T
NG_055295.1:g.6631G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.448G>T	ENSP00000476098.1:p.Ala150Ser
ENST00000610963.1:c.447G>T	ENSP00000481371.1:p.Ser149=
ENST00000616270.4:c.422+242G>T	ENSP00000480679.1:n.422+242G>T
ENST00000634680.1:c.232G>T	ENSP00000489240.1:p.Ala78Ser
ENST00000634967.1:c.304G>T	ENSP00000489559.1:p.Ala102Ser
NR_074079.1:n.725G>T