Canonical Allele Identifier: CA405755367

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738169G>T (hg19) ; chr19:g.39247529G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247529G>T , CM000681.2:g.39247529G>T	GRCh38
NC_000019.9:g.39738169G>T , CM000681.1:g.39738169G>T	GRCh37
NC_000019.8:g.44430009G>T	NCBI36
NG_042193.1:g.2443C>A
NG_055295.1:g.6328C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.368-66C>A	ENSP00000476098.1:n.368-66C>A
ENST00000610963.1:c.367-66C>A	ENSP00000481371.1:n.367-66C>A
ENST00000616270.4:c.361C>A	ENSP00000480679.1:p.His121Asn
ENST00000634680.1:c.152-66C>A	ENSP00000489240.1:n.152-66C>A
ENST00000634967.1:c.224-66C>A	ENSP00000489559.1:n.224-66C>A
NR_074079.1:n.645-66C>A