Canonical Allele Identifier: CA507407698

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738468C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247828C>G , CM000681.2:g.39247828C>G	GRCh38
NC_000019.9:g.39738468C>G , CM000681.1:g.39738468C>G	GRCh37
NC_000019.8:g.44430308C>G	NCBI36
NG_042193.1:g.2144G>C
NG_055295.1:g.6029G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.247G>C	ENSP00000476098.1:p.Gly83Arg
ENST00000610963.1:c.246G>C	ENSP00000481371.1:p.Val82=
ENST00000616270.4:c.223+96G>C	ENSP00000480679.1:n.223+96G>C
ENST00000634680.1:c.152-365G>C	ENSP00000489240.1:n.152-365G>C
ENST00000634967.1:c.223+96G>C	ENSP00000489559.1:n.223+96G>C
NR_074079.1:n.524G>C