Canonical Allele Identifier: CA2335423736
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs1302521475

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247870G>A , CM000681.2:g.39247870G>A GRCh38
NC_000019.9:g.39738510G>A , CM000681.1:g.39738510G>A GRCh37
NC_000019.8:g.44430350G>A NCBI36
NG_042193.1:g.2102C>T
NG_055295.1:g.5987C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.224-19C>T ENSP00000476098.1:n.224-19C>T
ENST00000610963.1:c.223-19C>T ENSP00000481371.1:n.223-19C>T
ENST00000616270.4:c.223+54C>T ENSP00000480679.1:n.223+54C>T
ENST00000634680.1:c.152-407C>T ENSP00000489240.1:n.152-407C>T
ENST00000634967.1:c.223+54C>T ENSP00000489559.1:n.223+54C>T
NR_074079.1:n.501-19C>T