Canonical Allele Identifier: CA507407469

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738365T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247725T>G , CM000681.2:g.39247725T>G	GRCh38
NC_000019.9:g.39738365T>G , CM000681.1:g.39738365T>G	GRCh37
NC_000019.8:g.44430205T>G	NCBI36
NG_042193.1:g.2247A>C
NG_055295.1:g.6132A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.350A>C	ENSP00000476098.1:p.Glu117Ala
ENST00000610963.1:c.349A>C	ENSP00000481371.1:p.Arg117=
ENST00000616270.4:c.224-59A>C	ENSP00000480679.1:n.224-59A>C
ENST00000634680.1:c.152-262A>C	ENSP00000489240.1:n.152-262A>C
ENST00000634967.1:c.223+199A>C	ENSP00000489559.1:n.223+199A>C
NR_074079.1:n.627A>C