Canonical Allele Identifier: CA405755752

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738262T>C (hg19) ; chr19:g.39247622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247622T>C , CM000681.2:g.39247622T>C	GRCh38
NC_000019.9:g.39738262T>C , CM000681.1:g.39738262T>C	GRCh37
NC_000019.8:g.44430102T>C	NCBI36
NG_042193.1:g.2350A>G
NG_055295.1:g.6235A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+86A>G	ENSP00000476098.1:n.367+86A>G
ENST00000610963.1:c.366+86A>G	ENSP00000481371.1:n.366+86A>G
ENST00000616270.4:c.268A>G	ENSP00000480679.1:p.Asn90Asp
ENST00000634680.1:c.152-159A>G	ENSP00000489240.1:n.152-159A>G
ENST00000634967.1:c.224-159A>G	ENSP00000489559.1:n.224-159A>G
NR_074079.1:n.644+86A>G