Canonical Allele Identifier: CA405756638

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247936-A-G
• MyVariant Identifiers: chr19:g.39738576A>G (hg19) ; chr19:g.39247936A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247936A>G , CM000681.2:g.39247936A>G	GRCh38
NC_000019.9:g.39738576A>G , CM000681.1:g.39738576A>G	GRCh37
NC_000019.8:g.44430416A>G	NCBI36
NG_042193.1:g.2036T>C
NG_055295.1:g.5921T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.211T>C	ENSP00000476098.1:p.Ser71Pro
ENST00000610963.1:c.210T>C	ENSP00000481371.1:p.Pro70=
ENST00000616270.4:c.211T>C	ENSP00000480679.1:p.Ser71Pro
ENST00000634680.1:c.152-473T>C	ENSP00000489240.1:n.152-473T>C
ENST00000634967.1:c.211T>C	ENSP00000489559.1:p.Ser71Pro
NR_074079.1:n.488T>C