Canonical Allele Identifier: CA405756634

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247935-G-T
• MyVariant Identifiers: chr19:g.39738575G>T (hg19) ; chr19:g.39247935G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247935G>T , CM000681.2:g.39247935G>T	GRCh38
NC_000019.9:g.39738575G>T , CM000681.1:g.39738575G>T	GRCh37
NC_000019.8:g.44430415G>T	NCBI36
NG_042193.1:g.2037C>A
NG_055295.1:g.5922C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.212C>A	ENSP00000476098.1:p.Ser71Tyr
ENST00000610963.1:c.211C>A	ENSP00000481371.1:p.Pro71Thr
ENST00000616270.4:c.212C>A	ENSP00000480679.1:p.Ser71Tyr
ENST00000634680.1:c.152-472C>A	ENSP00000489240.1:n.152-472C>A
ENST00000634967.1:c.212C>A	ENSP00000489559.1:p.Ser71Tyr
NR_074079.1:n.489C>A