Canonical Allele Identifier: CA507655500

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738101A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247461A>C , CM000681.2:g.39247461A>C	GRCh38
NC_000019.9:g.39738101A>C , CM000681.1:g.39738101A>C	GRCh37
NC_000019.8:g.44429941A>C	NCBI36
NG_042193.1:g.2511T>G
NG_055295.1:g.6396T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.370T>G	ENSP00000476098.1:p.Ter124Gly
ENST00000610963.1:c.369T>G	ENSP00000481371.1:p.Leu123=
ENST00000616270.4:c.422+7T>G	ENSP00000480679.1:n.422+7T>G
ENST00000634680.1:c.154T>G	ENSP00000489240.1:p.Ter52Gly
ENST00000634967.1:c.226T>G	ENSP00000489559.1:p.Ter76Gly
NR_074079.1:n.647T>G