Canonical Allele Identifier: CA507407520

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247741-C-G
• MyVariant Identifiers: chr19:g.39738381C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247741C>G , CM000681.2:g.39247741C>G	GRCh38
NC_000019.9:g.39738381C>G , CM000681.1:g.39738381C>G	GRCh37
NC_000019.8:g.44430221C>G	NCBI36
NG_042193.1:g.2231G>C
NG_055295.1:g.6116G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.334G>C	ENSP00000476098.1:p.Ala112Pro
ENST00000610963.1:c.333G>C	ENSP00000481371.1:p.Leu111=
ENST00000616270.4:c.224-75G>C	ENSP00000480679.1:n.224-75G>C
ENST00000634680.1:c.152-278G>C	ENSP00000489240.1:n.152-278G>C
ENST00000634967.1:c.223+183G>C	ENSP00000489559.1:n.223+183G>C
NR_074079.1:n.611G>C