Canonical Allele Identifier: CA405756679

Gene: IFNL4

Linked Data

• dbSNP Id: rs2074957068
• gnomAD v4: 19-39247944-T-C
• MyVariant Identifiers: chr19:g.39738584T>C (hg19) ; chr19:g.39247944T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247944T>C , CM000681.2:g.39247944T>C	GRCh38
NC_000019.9:g.39738584T>C , CM000681.1:g.39738584T>C	GRCh37
NC_000019.8:g.44430424T>C	NCBI36
NG_042193.1:g.2028A>G
NG_055295.1:g.5913A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.203A>G	ENSP00000476098.1:p.Glu68Gly
ENST00000610963.1:c.202A>G	ENSP00000481371.1:p.Arg68Gly
ENST00000616270.4:c.203A>G	ENSP00000480679.1:p.Glu68Gly
ENST00000634680.1:c.152-481A>G	ENSP00000489240.1:n.152-481A>G
ENST00000634967.1:c.203A>G	ENSP00000489559.1:p.Glu68Gly
NR_074079.1:n.480A>G