Canonical Allele Identifier: CA2506351233
Gene: IFNL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247894_39247913dup , CM000681.2:g.39247894_39247913dup GRCh38
NC_000019.9:g.39738534_39738553dup , CM000681.1:g.39738534_39738553dup GRCh37
NC_000019.8:g.44430374_44430393dup NCBI36
NG_042193.1:g.2061_2080dup
NG_055295.1:g.5946_5965dup

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.223+13_223+32dup ENSP00000476098.1:n.223+13_223+32dup
ENST00000610963.1:c.222+13_222+32dup ENSP00000481371.1:n.222+13_222+32dup
ENST00000616270.4:c.223+13_223+32dup ENSP00000480679.1:n.223+13_223+32dup
ENST00000634680.1:c.152-448_152-429dup ENSP00000489240.1:n.152-448_152-429dup
ENST00000634967.1:c.223+13_223+32dup ENSP00000489559.1:n.223+13_223+32dup
NR_074079.1:n.500+13_500+32dup