Canonical Allele Identifier: CA882119507
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs1266517387

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248205dup , CM000681.2:g.39248205dup GRCh38
NC_000019.9:g.39738845dup , CM000681.1:g.39738845dup GRCh37
NC_000019.8:g.44430685dup NCBI36
NG_042193.1:g.1768dup
NG_055295.1:g.5653dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.152-209dup ENSP00000476098.1:n.152-209dup
ENST00000610963.1:c.151-209dup ENSP00000481371.1:n.151-209dup
ENST00000616270.4:c.152-209dup ENSP00000480679.1:n.152-209dup
ENST00000634680.1:c.151+225dup ENSP00000489240.1:n.151+225dup
ENST00000634967.1:c.152-209dup ENSP00000489559.1:n.152-209dup
NR_074079.1:n.429-209dup