Canonical Allele Identifier: CA507655475

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738083G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247443G>A , CM000681.2:g.39247443G>A	GRCh38
NC_000019.9:g.39738083G>A , CM000681.1:g.39738083G>A	GRCh37
NC_000019.8:g.44429923G>A	NCBI36
NG_042193.1:g.2529C>T
NG_055295.1:g.6414C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.388C>T	ENSP00000476098.1:p.Leu130Phe
ENST00000610963.1:c.387C>T	ENSP00000481371.1:p.Gly129=
ENST00000616270.4:c.422+25C>T	ENSP00000480679.1:n.422+25C>T
ENST00000634680.1:c.172C>T	ENSP00000489240.1:p.Leu58Phe
ENST00000634967.1:c.244C>T	ENSP00000489559.1:p.Leu82Phe
NR_074079.1:n.665C>T