Canonical Allele Identifier: CA507407636

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738447G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247807G>T , CM000681.2:g.39247807G>T	GRCh38
NC_000019.9:g.39738447G>T , CM000681.1:g.39738447G>T	GRCh37
NC_000019.8:g.44430287G>T	NCBI36
NG_042193.1:g.2165C>A
NG_055295.1:g.6050C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.268C>A	ENSP00000476098.1:p.Pro90Thr
ENST00000610963.1:c.267C>A	ENSP00000481371.1:p.Ala89=
ENST00000616270.4:c.223+117C>A	ENSP00000480679.1:n.223+117C>A
ENST00000634680.1:c.152-344C>A	ENSP00000489240.1:n.152-344C>A
ENST00000634967.1:c.223+117C>A	ENSP00000489559.1:n.223+117C>A
NR_074079.1:n.545C>A