Canonical Allele Identifier: CA507655499

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738098C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247458C>T , CM000681.2:g.39247458C>T	GRCh38
NC_000019.9:g.39738098C>T , CM000681.1:g.39738098C>T	GRCh37
NC_000019.8:g.44429938C>T	NCBI36
NG_042193.1:g.2514G>A
NG_055295.1:g.6399G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.373G>A	ENSP00000476098.1:p.Ala125Thr
ENST00000610963.1:c.372G>A	ENSP00000481371.1:p.Glu124=
ENST00000616270.4:c.422+10G>A	ENSP00000480679.1:n.422+10G>A
ENST00000634680.1:c.157G>A	ENSP00000489240.1:p.Ala53Thr
ENST00000634967.1:c.229G>A	ENSP00000489559.1:p.Ala77Thr
NR_074079.1:n.650G>A