Canonical Allele Identifier: CA308189524

Gene: IFNL4

Linked Data

• dbSNP Id: rs1037345367
• gnomAD v3: 19-39247992-C-T
• gnomAD v4: 19-39247992-C-T
• MyVariant Identifiers: chr19:g.39738632C>T (hg19) ; chr19:g.39247992C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247992C>T , CM000681.2:g.39247992C>T	GRCh38
NC_000019.9:g.39738632C>T , CM000681.1:g.39738632C>T	GRCh37
NC_000019.8:g.44430472C>T	NCBI36
NG_042193.1:g.1980G>A
NG_055295.1:g.5865G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.155G>A	ENSP00000476098.1:p.Gly52Glu
ENST00000610963.1:c.154G>A	ENSP00000481371.1:p.Glu52Lys
ENST00000616270.4:c.155G>A	ENSP00000480679.1:p.Gly52Glu
ENST00000634680.1:c.151+437G>A	ENSP00000489240.1:n.151+437G>A
ENST00000634967.1:c.155G>A	ENSP00000489559.1:p.Gly52Glu
NR_074079.1:n.432G>A