Canonical Allele Identifier: CA882119439
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs1381748124

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248038C>A , CM000681.2:g.39248038C>A GRCh38
NC_000019.9:g.39738678C>A , CM000681.1:g.39738678C>A GRCh37
NC_000019.8:g.44430518C>A NCBI36
NG_042193.1:g.1934G>T
NG_055295.1:g.5819G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-43G>T ENSP00000476098.1:n.152-43G>T
ENST00000610963.1:c.151-43G>T ENSP00000481371.1:n.151-43G>T
ENST00000616270.4:c.152-43G>T ENSP00000480679.1:n.152-43G>T
ENST00000634680.1:c.151+391G>T ENSP00000489240.1:n.151+391G>T
ENST00000634967.1:c.152-43G>T ENSP00000489559.1:n.152-43G>T
NR_074079.1:n.429-43G>T