Canonical Allele Identifier: CA308189769
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs943167505

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248254G>A , CM000681.2:g.39248254G>A GRCh38
NC_000019.9:g.39738894G>A , CM000681.1:g.39738894G>A GRCh37
NC_000019.8:g.44430734G>A NCBI36
NG_042193.1:g.1718C>T
NG_055295.1:g.5603C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.151+175C>T ENSP00000476098.1:n.151+175C>T
ENST00000610963.1:c.150+175C>T ENSP00000481371.1:n.150+175C>T
ENST00000616270.4:c.151+175C>T ENSP00000480679.1:n.151+175C>T
ENST00000634680.1:c.151+175C>T ENSP00000489240.1:n.151+175C>T
ENST00000634967.1:c.151+175C>T ENSP00000489559.1:n.151+175C>T
NR_074079.1:n.428+175C>T