Canonical Allele Identifier: CA405755185
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs533259477

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247490A>G , CM000681.2:g.39247490A>G GRCh38
NC_000019.9:g.39738130A>G , CM000681.1:g.39738130A>G GRCh37
NC_000019.8:g.44429970A>G NCBI36
NG_042193.1:g.2482T>C
NG_055295.1:g.6367T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.368-27T>C ENSP00000476098.1:n.368-27T>C
ENST00000610963.1:c.367-27T>C ENSP00000481371.1:n.367-27T>C
ENST00000616270.4:c.400T>C ENSP00000480679.1:p.Ser134Pro
ENST00000634680.1:c.152-27T>C ENSP00000489240.1:n.152-27T>C
ENST00000634967.1:c.224-27T>C ENSP00000489559.1:n.224-27T>C
NR_074079.1:n.645-27T>C