Canonical Allele Identifier: CA507655489

Gene: IFNL4

Linked Data

• dbSNP Id: rs1476005094
• gnomAD v3: 19-39247449-C-A
• gnomAD v4: 19-39247449-C-A
• MyVariant Identifiers: chr19:g.39738089C>A (hg19) ; chr19:g.39247449C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247449C>A , CM000681.2:g.39247449C>A	GRCh38
NC_000019.9:g.39738089C>A , CM000681.1:g.39738089C>A	GRCh37
NC_000019.8:g.44429929C>A	NCBI36
NG_042193.1:g.2523G>T
NG_055295.1:g.6408G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.382G>T	ENSP00000476098.1:p.Ala128Ser
ENST00000610963.1:c.381G>T	ENSP00000481371.1:p.Arg127=
ENST00000616270.4:c.422+19G>T	ENSP00000480679.1:n.422+19G>T
ENST00000634680.1:c.166G>T	ENSP00000489240.1:p.Ala56Ser
ENST00000634967.1:c.238G>T	ENSP00000489559.1:p.Ala80Ser
NR_074079.1:n.659G>T