Canonical Allele Identifier: CA882119201

Gene: IFNL4

Linked Data

• dbSNP Id: rs1361772597
• MyVariant Identifiers: chr19:g.39738520G>A (hg19) ; chr19:g.39247880G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247880G>A , CM000681.2:g.39247880G>A	GRCh38
NC_000019.9:g.39738520G>A , CM000681.1:g.39738520G>A	GRCh37
NC_000019.8:g.44430360G>A	NCBI36
NG_042193.1:g.2092C>T
NG_055295.1:g.5977C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.224-29C>T	ENSP00000476098.1:n.224-29C>T
ENST00000610963.1:c.223-29C>T	ENSP00000481371.1:n.223-29C>T
ENST00000616270.4:c.223+44C>T	ENSP00000480679.1:n.223+44C>T
ENST00000634680.1:c.152-417C>T	ENSP00000489240.1:n.152-417C>T
ENST00000634967.1:c.223+44C>T	ENSP00000489559.1:n.223+44C>T
NR_074079.1:n.501-29C>T