Canonical Allele Identifier: CA308189675
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs918888648

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248177C>T , CM000681.2:g.39248177C>T GRCh38
NC_000019.9:g.39738817C>T , CM000681.1:g.39738817C>T GRCh37
NC_000019.8:g.44430657C>T NCBI36
NG_042193.1:g.1795G>A
NG_055295.1:g.5680G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-182G>A ENSP00000476098.1:n.152-182G>A
ENST00000610963.1:c.151-182G>A ENSP00000481371.1:n.151-182G>A
ENST00000616270.4:c.152-182G>A ENSP00000480679.1:n.152-182G>A
ENST00000634680.1:c.151+252G>A ENSP00000489240.1:n.151+252G>A
ENST00000634967.1:c.152-182G>A ENSP00000489559.1:n.152-182G>A
NR_074079.1:n.429-182G>A