Canonical Allele Identifier: CA507655477

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738083G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247443G>C , CM000681.2:g.39247443G>C	GRCh38
NC_000019.9:g.39738083G>C , CM000681.1:g.39738083G>C	GRCh37
NC_000019.8:g.44429923G>C	NCBI36
NG_042193.1:g.2529C>G
NG_055295.1:g.6414C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.388C>G	ENSP00000476098.1:p.Leu130Val
ENST00000610963.1:c.387C>G	ENSP00000481371.1:p.Gly129=
ENST00000616270.4:c.422+25C>G	ENSP00000480679.1:n.422+25C>G
ENST00000634680.1:c.172C>G	ENSP00000489240.1:p.Leu58Val
ENST00000634967.1:c.244C>G	ENSP00000489559.1:p.Leu82Val
NR_074079.1:n.665C>G