Canonical Allele Identifier: CA405756002

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247715-G-C
• MyVariant Identifiers: chr19:g.39738355G>C (hg19) ; chr19:g.39247715G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247715G>C , CM000681.2:g.39247715G>C	GRCh38
NC_000019.9:g.39738355G>C , CM000681.1:g.39738355G>C	GRCh37
NC_000019.8:g.44430195G>C	NCBI36
NG_042193.1:g.2257C>G
NG_055295.1:g.6142C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.360C>G	ENSP00000476098.1:p.Gly120=
ENST00000610963.1:c.359C>G	ENSP00000481371.1:p.Ala120Gly
ENST00000616270.4:c.224-49C>G	ENSP00000480679.1:n.224-49C>G
ENST00000634680.1:c.152-252C>G	ENSP00000489240.1:n.152-252C>G
ENST00000634967.1:c.223+209C>G	ENSP00000489559.1:n.223+209C>G
NR_074079.1:n.637C>G