Canonical Allele Identifier: CA507655470

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738080G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247440G>C , CM000681.2:g.39247440G>C	GRCh38
NC_000019.9:g.39738080G>C , CM000681.1:g.39738080G>C	GRCh37
NC_000019.8:g.44429920G>C	NCBI36
NG_042193.1:g.2532C>G
NG_055295.1:g.6417C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.391C>G	ENSP00000476098.1:p.Leu131Val
ENST00000610963.1:c.390C>G	ENSP00000481371.1:p.Ser130=
ENST00000616270.4:c.422+28C>G	ENSP00000480679.1:n.422+28C>G
ENST00000634680.1:c.175C>G	ENSP00000489240.1:p.Leu59Val
ENST00000634967.1:c.247C>G	ENSP00000489559.1:p.Leu83Val
NR_074079.1:n.668C>G