Canonical Allele Identifier: CA405755045

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247460-C-G
• MyVariant Identifiers: chr19:g.39738100C>G (hg19) ; chr19:g.39247460C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247460C>G , CM000681.2:g.39247460C>G	GRCh38
NC_000019.9:g.39738100C>G , CM000681.1:g.39738100C>G	GRCh37
NC_000019.8:g.44429940C>G	NCBI36
NG_042193.1:g.2512G>C
NG_055295.1:g.6397G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.371G>C	ENSP00000476098.1:p.Ter124Ser
ENST00000610963.1:c.370G>C	ENSP00000481371.1:p.Glu124Gln
ENST00000616270.4:c.422+8G>C	ENSP00000480679.1:n.422+8G>C
ENST00000634680.1:c.155G>C	ENSP00000489240.1:p.Ter52Ser
ENST00000634967.1:c.227G>C	ENSP00000489559.1:p.Ter76Ser
NR_074079.1:n.648G>C