Canonical Allele Identifier: CA2335423767
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247909A= , CM000681.2:g.39247909A= GRCh38
NC_000019.9:g.39738549A= , CM000681.1:g.39738549A= GRCh37
NC_000019.8:g.44430389A= NCBI36
NG_042193.1:g.2063T=
NG_055295.1:g.5948T=

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.223+15T= ENSP00000476098.1:n.223+15T=
ENST00000610963.1:c.222+15T= ENSP00000481371.1:n.222+15T=
ENST00000616270.4:c.223+15T= ENSP00000480679.1:n.223+15T=
ENST00000634680.1:c.152-446T= ENSP00000489240.1:n.152-446T=
ENST00000634967.1:c.223+15T= ENSP00000489559.1:n.223+15T=
NR_074079.1:n.500+15T=