Canonical Allele Identifier: CA405756145

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738391A>C (hg19) ; chr19:g.39247751A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247751A>C , CM000681.2:g.39247751A>C	GRCh38
NC_000019.9:g.39738391A>C , CM000681.1:g.39738391A>C	GRCh37
NC_000019.8:g.44430231A>C	NCBI36
NG_042193.1:g.2221T>G
NG_055295.1:g.6106T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.324T>G	ENSP00000476098.1:p.Asp108Glu
ENST00000610963.1:c.323T>G	ENSP00000481371.1:p.Ile108Ser
ENST00000616270.4:c.224-85T>G	ENSP00000480679.1:n.224-85T>G
ENST00000634680.1:c.152-288T>G	ENSP00000489240.1:n.152-288T>G
ENST00000634967.1:c.223+173T>G	ENSP00000489559.1:n.223+173T>G
NR_074079.1:n.601T>G