Canonical Allele Identifier: CA405756666

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738581C>T (hg19) ; chr19:g.39247941C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247941C>T , CM000681.2:g.39247941C>T	GRCh38
NC_000019.9:g.39738581C>T , CM000681.1:g.39738581C>T	GRCh37
NC_000019.8:g.44430421C>T	NCBI36
NG_042193.1:g.2031G>A
NG_055295.1:g.5916G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.206G>A	ENSP00000476098.1:p.Gly69Glu
ENST00000610963.1:c.205G>A	ENSP00000481371.1:p.Asp69Asn
ENST00000616270.4:c.206G>A	ENSP00000480679.1:p.Gly69Glu
ENST00000634680.1:c.152-478G>A	ENSP00000489240.1:n.152-478G>A
ENST00000634967.1:c.206G>A	ENSP00000489559.1:p.Gly69Glu
NR_074079.1:n.483G>A