Canonical Allele Identifier: CA507407588

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738429G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247789G>C , CM000681.2:g.39247789G>C	GRCh38
NC_000019.9:g.39738429G>C , CM000681.1:g.39738429G>C	GRCh37
NC_000019.8:g.44430269G>C	NCBI36
NG_042193.1:g.2183C>G
NG_055295.1:g.6068C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.286C>G	ENSP00000476098.1:p.Pro96Ala
ENST00000610963.1:c.285C>G	ENSP00000481371.1:p.Gly95=
ENST00000616270.4:c.224-123C>G	ENSP00000480679.1:n.224-123C>G
ENST00000634680.1:c.152-326C>G	ENSP00000489240.1:n.152-326C>G
ENST00000634967.1:c.223+135C>G	ENSP00000489559.1:n.223+135C>G
NR_074079.1:n.563C>G