Canonical Allele Identifier: CA405756938

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247991-T-C
• MyVariant Identifiers: chr19:g.39738631T>C (hg19) ; chr19:g.39247991T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247991T>C , CM000681.2:g.39247991T>C	GRCh38
NC_000019.9:g.39738631T>C , CM000681.1:g.39738631T>C	GRCh37
NC_000019.8:g.44430471T>C	NCBI36
NG_042193.1:g.1981A>G
NG_055295.1:g.5866A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.156A>G	ENSP00000476098.1:p.Gly52=
ENST00000610963.1:c.155A>G	ENSP00000481371.1:p.Glu52Gly
ENST00000616270.4:c.156A>G	ENSP00000480679.1:p.Gly52=
ENST00000634680.1:c.151+438A>G	ENSP00000489240.1:n.151+438A>G
ENST00000634967.1:c.156A>G	ENSP00000489559.1:p.Gly52=
NR_074079.1:n.433A>G