Canonical Allele Identifier: CA405756499

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074956355
• gnomAD v4: 19-39247841-C-A
• MyVariant Identifiers: chr19:g.39738481C>A (hg19) ; chr19:g.39247841C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247841C>A , CM000681.2:g.39247841C>A	GRCh38
NC_000019.9:g.39738481C>A , CM000681.1:g.39738481C>A	GRCh37
NC_000019.8:g.44430321C>A	NCBI36
NG_042193.1:g.2131G>T
NG_055295.1:g.6016G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.234G>T	ENSP00000476098.1:p.Ser78=
ENST00000610963.1:c.233G>T	ENSP00000481371.1:p.Arg78Leu
ENST00000616270.4:c.223+83G>T	ENSP00000480679.1:n.223+83G>T
ENST00000634680.1:c.152-378G>T	ENSP00000489240.1:n.152-378G>T
ENST00000634967.1:c.223+83G>T	ENSP00000489559.1:n.223+83G>T
NR_074079.1:n.511G>T