Canonical Allele Identifier: CA405756602

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247930-C-A
• MyVariant Identifiers: chr19:g.39738570C>A (hg19) ; chr19:g.39247930C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247930C>A , CM000681.2:g.39247930C>A	GRCh38
NC_000019.9:g.39738570C>A , CM000681.1:g.39738570C>A	GRCh37
NC_000019.8:g.44430410C>A	NCBI36
NG_042193.1:g.2042G>T
NG_055295.1:g.5927G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.217G>T	ENSP00000476098.1:p.Ala73Ser
ENST00000610963.1:c.216G>T	ENSP00000481371.1:p.Arg72=
ENST00000616270.4:c.217G>T	ENSP00000480679.1:p.Ala73Ser
ENST00000634680.1:c.152-467G>T	ENSP00000489240.1:n.152-467G>T
ENST00000634967.1:c.217G>T	ENSP00000489559.1:p.Ala73Ser
NR_074079.1:n.494G>T