Canonical Allele Identifier: CA405756870

Gene: IFNL4

Linked Data

• dbSNP Id: rs1334279357
• gnomAD v4: 19-39247979-C-G
• MyVariant Identifiers: chr19:g.39738619C>G (hg19) ; chr19:g.39247979C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247979C>G , CM000681.2:g.39247979C>G	GRCh38
NC_000019.9:g.39738619C>G , CM000681.1:g.39738619C>G	GRCh37
NC_000019.8:g.44430459C>G	NCBI36
NG_042193.1:g.1993G>C
NG_055295.1:g.5878G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.168G>C	ENSP00000476098.1:p.Glu56Asp
ENST00000610963.1:c.167G>C	ENSP00000481371.1:p.Ser56Thr
ENST00000616270.4:c.168G>C	ENSP00000480679.1:p.Glu56Asp
ENST00000634680.1:c.151+450G>C	ENSP00000489240.1:n.151+450G>C
ENST00000634967.1:c.168G>C	ENSP00000489559.1:p.Glu56Asp
NR_074079.1:n.445G>C