Canonical Allele Identifier: CA995767130

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074955059
• gnomAD v3: 19-39247638-CTCGCCGTGGGCCTG-C
• gnomAD v4: 19-39247638-CTCGCCGTGGGCCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247639_39247652del , CM000681.2:g.39247639_39247652del	GRCh38
NC_000019.9:g.39738279_39738292del , CM000681.1:g.39738279_39738292del	GRCh37
NC_000019.8:g.44430119_44430132del	NCBI36
NG_042193.1:g.2320_2333del
NG_055295.1:g.6205_6218del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+56_367+69del	ENSP00000476098.1:n.367+56_367+69del
ENST00000610963.1:c.366+56_366+69del	ENSP00000481371.1:n.366+56_366+69del
ENST00000616270.4:c.238_251del	ENSP00000480679.1:p.Gln80AlafsTer26
ENST00000634680.1:c.152-189_152-176del	ENSP00000489240.1:n.152-189_152-176del
ENST00000634967.1:c.224-189_224-176del	ENSP00000489559.1:n.224-189_224-176del
NR_074079.1:n.644+56_644+69del