Canonical Allele Identifier: CA2335423947

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074958609

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39248256_39248257dup , CM000681.2:g.39248256_39248257dup	GRCh38
NC_000019.9:g.39738896_39738897dup , CM000681.1:g.39738896_39738897dup	GRCh37
NC_000019.8:g.44430736_44430737dup	NCBI36
NG_042193.1:g.1715_1716dup
NG_055295.1:g.5600_5601dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.151+172_151+173dup	ENSP00000476098.1:n.151+172_151+173dup
ENST00000610963.1:c.150+172_150+173dup	ENSP00000481371.1:n.150+172_150+173dup
ENST00000616270.4:c.151+172_151+173dup	ENSP00000480679.1:n.151+172_151+173dup
ENST00000634680.1:c.151+172_151+173dup	ENSP00000489240.1:n.151+172_151+173dup
ENST00000634967.1:c.151+172_151+173dup	ENSP00000489559.1:n.151+172_151+173dup
NR_074079.1:n.428+172_428+173dup