Canonical Allele Identifier: CA308189176

Gene: IFNL4

Linked Data

• dbSNP Id: rs761613102
• MyVariant Identifiers: chr19:g.39738309_39738324del (hg19) ; chr19:g.39247669_39247684del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247676_39247691del , CM000681.2:g.39247676_39247691del	GRCh38
NC_000019.9:g.39738316_39738331del , CM000681.1:g.39738316_39738331del	GRCh37
NC_000019.8:g.44430156_44430171del	NCBI36
NG_042193.1:g.2288_2303del
NG_055295.1:g.6173_6188del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+24_367+39del	ENSP00000476098.1:n.367+24_367+39del
ENST00000610963.1:c.366+24_366+39del	ENSP00000481371.1:n.366+24_366+39del
ENST00000616270.4:c.224-18_224-3del	ENSP00000480679.1:n.224-18_224-3del
ENST00000634680.1:c.152-221_152-206del	ENSP00000489240.1:n.152-221_152-206del
ENST00000634967.1:c.224-221_224-206del	ENSP00000489559.1:n.224-221_224-206del
NR_074079.1:n.644+24_644+39del