Canonical Allele Identifier: CA405755857

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247645-T-C
• MyVariant Identifiers: chr19:g.39738285T>C (hg19) ; chr19:g.39247645T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247645T>C , CM000681.2:g.39247645T>C	GRCh38
NC_000019.9:g.39738285T>C , CM000681.1:g.39738285T>C	GRCh37
NC_000019.8:g.44430125T>C	NCBI36
NG_042193.1:g.2327A>G
NG_055295.1:g.6212A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.367+63A>G	ENSP00000476098.1:n.367+63A>G
ENST00000610963.1:c.366+63A>G	ENSP00000481371.1:n.366+63A>G
ENST00000616270.4:c.245A>G	ENSP00000480679.1:p.His82Arg
ENST00000634680.1:c.152-182A>G	ENSP00000489240.1:n.152-182A>G
ENST00000634967.1:c.224-182A>G	ENSP00000489559.1:n.224-182A>G
NR_074079.1:n.644+63A>G