Canonical Allele Identifier: CA405756110

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738383G>C (hg19) ; chr19:g.39247743G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247743G>C , CM000681.2:g.39247743G>C	GRCh38
NC_000019.9:g.39738383G>C , CM000681.1:g.39738383G>C	GRCh37
NC_000019.8:g.44430223G>C	NCBI36
NG_042193.1:g.2229C>G
NG_055295.1:g.6114C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.332C>G	ENSP00000476098.1:p.Ala111Gly
ENST00000610963.1:c.331C>G	ENSP00000481371.1:p.Leu111Val
ENST00000616270.4:c.224-77C>G	ENSP00000480679.1:n.224-77C>G
ENST00000634680.1:c.152-280C>G	ENSP00000489240.1:n.152-280C>G
ENST00000634967.1:c.223+181C>G	ENSP00000489559.1:n.223+181C>G
NR_074079.1:n.609C>G