Canonical Allele Identifier: CA405756884

Gene: IFNL4

Linked Data

• dbSNP Id: rs1432831692
• gnomAD v2: 19-39738621-C-T
• gnomAD v3: 19-39247981-C-T
• gnomAD v4: 19-39247981-C-T
• MyVariant Identifiers: chr19:g.39738621C>T (hg19) ; chr19:g.39247981C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247981C>T , CM000681.2:g.39247981C>T	GRCh38
NC_000019.9:g.39738621C>T , CM000681.1:g.39738621C>T	GRCh37
NC_000019.8:g.44430461C>T	NCBI36
NG_042193.1:g.1991G>A
NG_055295.1:g.5876G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.166G>A	ENSP00000476098.1:p.Glu56Lys
ENST00000610963.1:c.165G>A	ENSP00000481371.1:p.Leu55=
ENST00000616270.4:c.166G>A	ENSP00000480679.1:p.Glu56Lys
ENST00000634680.1:c.151+448G>A	ENSP00000489240.1:n.151+448G>A
ENST00000634967.1:c.166G>A	ENSP00000489559.1:p.Glu56Lys
NR_074079.1:n.443G>A