Canonical Allele Identifier: CA405756931

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738630T>G (hg19) ; chr19:g.39247990T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247990T>G , CM000681.2:g.39247990T>G	GRCh38
NC_000019.9:g.39738630T>G , CM000681.1:g.39738630T>G	GRCh37
NC_000019.8:g.44430470T>G	NCBI36
NG_042193.1:g.1982A>C
NG_055295.1:g.5867A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.157A>C	ENSP00000476098.1:p.Arg53=
ENST00000610963.1:c.156A>C	ENSP00000481371.1:p.Glu52Asp
ENST00000616270.4:c.157A>C	ENSP00000480679.1:p.Arg53=
ENST00000634680.1:c.151+439A>C	ENSP00000489240.1:n.151+439A>C
ENST00000634967.1:c.157A>C	ENSP00000489559.1:p.Arg53=
NR_074079.1:n.434A>C