Canonical Allele Identifier: CA995767121

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074955044
• gnomAD v3: 19-39247632-CTGGGG-C
• gnomAD v4: 19-39247632-CTGGGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247633_39247637del , CM000681.2:g.39247633_39247637del	GRCh38
NC_000019.9:g.39738273_39738277del , CM000681.1:g.39738273_39738277del	GRCh37
NC_000019.8:g.44430113_44430117del	NCBI36
NG_042193.1:g.2335_2339del
NG_055295.1:g.6220_6224del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+71_367+75del	ENSP00000476098.1:n.367+71_367+75del
ENST00000610963.1:c.366+71_366+75del	ENSP00000481371.1:n.366+71_366+75del
ENST00000616270.4:c.253_257del	ENSP00000480679.1:p.Pro85AlafsTer24
ENST00000634680.1:c.152-174_152-170del	ENSP00000489240.1:n.152-174_152-170del
ENST00000634967.1:c.224-174_224-170del	ENSP00000489559.1:n.224-174_224-170del
NR_074079.1:n.644+71_644+75del