Canonical Allele Identifier: CA507407759

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247849-G-T
• MyVariant Identifiers: chr19:g.39738489G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247849G>T , CM000681.2:g.39247849G>T	GRCh38
NC_000019.9:g.39738489G>T , CM000681.1:g.39738489G>T	GRCh37
NC_000019.8:g.44430329G>T	NCBI36
NG_042193.1:g.2123C>A
NG_055295.1:g.6008C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.226C>A	ENSP00000476098.1:p.Leu76Met
ENST00000610963.1:c.225C>A	ENSP00000481371.1:p.Ser75=
ENST00000616270.4:c.223+75C>A	ENSP00000480679.1:n.223+75C>A
ENST00000634680.1:c.152-386C>A	ENSP00000489240.1:n.152-386C>A
ENST00000634967.1:c.223+75C>A	ENSP00000489559.1:n.223+75C>A
NR_074079.1:n.503C>A