Canonical Allele Identifier: CA507655492

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738092T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247452T>A , CM000681.2:g.39247452T>A	GRCh38
NC_000019.9:g.39738092T>A , CM000681.1:g.39738092T>A	GRCh37
NC_000019.8:g.44429932T>A	NCBI36
NG_042193.1:g.2520A>T
NG_055295.1:g.6405A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.379A>T	ENSP00000476098.1:p.Thr127Ser
ENST00000610963.1:c.378A>T	ENSP00000481371.1:p.Ala126=
ENST00000616270.4:c.422+16A>T	ENSP00000480679.1:n.422+16A>T
ENST00000634680.1:c.163A>T	ENSP00000489240.1:p.Thr55Ser
ENST00000634967.1:c.235A>T	ENSP00000489559.1:p.Thr79Ser
NR_074079.1:n.656A>T