Canonical Allele Identifier: CA405756532

Gene: IFNL4

Linked Data

• dbSNP Id: rs1428190393
• gnomAD v2: 19-39738488-A-T
• MyVariant Identifiers: chr19:g.39738488A>T (hg19) ; chr19:g.39247848A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247848A>T , CM000681.2:g.39247848A>T	GRCh38
NC_000019.9:g.39738488A>T , CM000681.1:g.39738488A>T	GRCh37
NC_000019.8:g.44430328A>T	NCBI36
NG_042193.1:g.2124T>A
NG_055295.1:g.6009T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.227T>A	ENSP00000476098.1:p.Leu76Gln
ENST00000610963.1:c.226T>A	ENSP00000481371.1:p.Cys76Ser
ENST00000616270.4:c.223+76T>A	ENSP00000480679.1:n.223+76T>A
ENST00000634680.1:c.152-385T>A	ENSP00000489240.1:n.152-385T>A
ENST00000634967.1:c.223+76T>A	ENSP00000489559.1:n.223+76T>A
NR_074079.1:n.504T>A