Canonical Allele Identifier: CA405755007

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738091G>C (hg19) ; chr19:g.39247451G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247451G>C , CM000681.2:g.39247451G>C	GRCh38
NC_000019.9:g.39738091G>C , CM000681.1:g.39738091G>C	GRCh37
NC_000019.8:g.44429931G>C	NCBI36
NG_042193.1:g.2521C>G
NG_055295.1:g.6406C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.380C>G	ENSP00000476098.1:p.Thr127Arg
ENST00000610963.1:c.379C>G	ENSP00000481371.1:p.Arg127Gly
ENST00000616270.4:c.422+17C>G	ENSP00000480679.1:n.422+17C>G
ENST00000634680.1:c.164C>G	ENSP00000489240.1:p.Thr55Arg
ENST00000634967.1:c.236C>G	ENSP00000489559.1:p.Thr79Arg
NR_074079.1:n.657C>G