Canonical Allele Identifier: CA405757360

Gene: IFNL4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39248489C>T , CM000681.2:g.39248489C>T	GRCh38
NC_000019.9:g.39739129C>T , CM000681.1:g.39739129C>T	GRCh37
NC_000019.8:g.44430969C>T	NCBI36
NG_042193.1:g.1483G>A
NG_055295.1:g.5368G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.91G>A	ENSP00000476098.1:p.Ala31Thr
ENST00000610963.1:c.90G>A	ENSP00000481371.1:p.Ser30=
ENST00000616270.4:c.91G>A	ENSP00000480679.1:p.Ala31Thr
ENST00000634680.1:c.91G>A	ENSP00000489240.1:p.Ala31Thr
ENST00000634967.1:c.91G>A	ENSP00000489559.1:p.Ala31Thr
NR_074079.1:n.368G>A