Canonical Allele Identifier: CA9426141

Gene: IFNL4

Linked Data

• dbSNP Id: rs142981501
• ExAC: 19:39738607 C / G
• gnomAD v2: 19-39738607-C-G
• gnomAD v3: 19-39247967-C-G
• gnomAD v4: 19-39247967-C-G
• MyVariant Identifiers: chr19:g.39738607C>G (hg19) ; chr19:g.39247967C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247967C>G , CM000681.2:g.39247967C>G	GRCh38
NC_000019.9:g.39738607C>G , CM000681.1:g.39738607C>G	GRCh37
NC_000019.8:g.44430447C>G	NCBI36
NG_042193.1:g.2005G>C
NG_055295.1:g.5890G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.180G>C	ENSP00000476098.1:p.Ala60=
ENST00000610963.1:c.179G>C	ENSP00000481371.1:p.Arg60Pro
ENST00000616270.4:c.180G>C	ENSP00000480679.1:p.Ala60=
ENST00000634680.1:c.151+462G>C	ENSP00000489240.1:n.151+462G>C
ENST00000634967.1:c.180G>C	ENSP00000489559.1:p.Ala60=
NR_074079.1:n.457G>C