Canonical Allele Identifier: CA882118892

Gene: IFNL4

Linked Data

• dbSNP Id: rs1284599038
• MyVariant Identifiers: chr19:g.39738273_39738295del (hg19) ; chr19:g.39247633_39247655del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247633_39247655del , CM000681.2:g.39247633_39247655del	GRCh38
NC_000019.9:g.39738273_39738295del , CM000681.1:g.39738273_39738295del	GRCh37
NC_000019.8:g.44430113_44430135del	NCBI36
NG_042193.1:g.2317_2339del
NG_055295.1:g.6202_6224del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+53_367+75del	ENSP00000476098.1:n.367+53_367+75del
ENST00000610963.1:c.366+53_366+75del	ENSP00000481371.1:n.366+53_366+75del
ENST00000616270.4:c.235_257del	ENSP00000480679.1:p.Pro79AlafsTer24
ENST00000634680.1:c.152-192_152-170del	ENSP00000489240.1:n.152-192_152-170del
ENST00000634967.1:c.224-192_224-170del	ENSP00000489559.1:n.224-192_224-170del
NR_074079.1:n.644+53_644+75del