Canonical Allele Identifier: CA507407537

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247750-G-A
• MyVariant Identifiers: chr19:g.39738390G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247750G>A , CM000681.2:g.39247750G>A	GRCh38
NC_000019.9:g.39738390G>A , CM000681.1:g.39738390G>A	GRCh37
NC_000019.8:g.44430230G>A	NCBI36
NG_042193.1:g.2222C>T
NG_055295.1:g.6107C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.325C>T	ENSP00000476098.1:p.Pro109Ser
ENST00000610963.1:c.324C>T	ENSP00000481371.1:p.Ile108=
ENST00000616270.4:c.224-84C>T	ENSP00000480679.1:n.224-84C>T
ENST00000634680.1:c.152-287C>T	ENSP00000489240.1:n.152-287C>T
ENST00000634967.1:c.223+174C>T	ENSP00000489559.1:n.223+174C>T
NR_074079.1:n.602C>T