Canonical Allele Identifier: CA995767373

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074956715
• gnomAD v3: 19-39247891-G-A
• gnomAD v4: 19-39247891-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247891G>A , CM000681.2:g.39247891G>A	GRCh38
NC_000019.9:g.39738531G>A , CM000681.1:g.39738531G>A	GRCh37
NC_000019.8:g.44430371G>A	NCBI36
NG_042193.1:g.2081C>T
NG_055295.1:g.5966C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.223+33C>T	ENSP00000476098.1:n.223+33C>T
ENST00000610963.1:c.222+33C>T	ENSP00000481371.1:n.222+33C>T
ENST00000616270.4:c.223+33C>T	ENSP00000480679.1:n.223+33C>T
ENST00000634680.1:c.152-428C>T	ENSP00000489240.1:n.152-428C>T
ENST00000634967.1:c.223+33C>T	ENSP00000489559.1:n.223+33C>T
NR_074079.1:n.500+33C>T