Canonical Allele Identifier: CA2335423599

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074954974

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247614G>A , CM000681.2:g.39247614G>A	GRCh38
NC_000019.9:g.39738254G>A , CM000681.1:g.39738254G>A	GRCh37
NC_000019.8:g.44430094G>A	NCBI36
NG_042193.1:g.2358C>T
NG_055295.1:g.6243C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+94C>T	ENSP00000476098.1:n.367+94C>T
ENST00000610963.1:c.366+94C>T	ENSP00000481371.1:n.366+94C>T
ENST00000616270.4:c.276C>T	ENSP00000480679.1:p.Ser92=
ENST00000634680.1:c.152-151C>T	ENSP00000489240.1:n.152-151C>T
ENST00000634967.1:c.224-151C>T	ENSP00000489559.1:n.224-151C>T
NR_074079.1:n.644+94C>T