Canonical Allele Identifier: CA995767483
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs2074957452

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248003del , CM000681.2:g.39248003del GRCh38
NC_000019.9:g.39738643del , CM000681.1:g.39738643del GRCh37
NC_000019.8:g.44430483del NCBI36
NG_042193.1:g.1969del
NG_055295.1:g.5854del

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-8del ENSP00000476098.1:n.152-8del
ENST00000610963.1:c.151-8del ENSP00000481371.1:n.151-8del
ENST00000616270.4:c.152-8del ENSP00000480679.1:n.152-8del
ENST00000634680.1:c.151+426del ENSP00000489240.1:n.151+426del
ENST00000634967.1:c.152-8del ENSP00000489559.1:n.152-8del
NR_074079.1:n.429-8del