Canonical Allele Identifier: CA308189514

Gene: IFNL4

Linked Data

• dbSNP Id: rs746231316
• gnomAD v4: 19-39247975-C-T
• MyVariant Identifiers: chr19:g.39738615C>T (hg19) ; chr19:g.39247975C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247975C>T , CM000681.2:g.39247975C>T	GRCh38
NC_000019.9:g.39738615C>T , CM000681.1:g.39738615C>T	GRCh37
NC_000019.8:g.44430455C>T	NCBI36
NG_042193.1:g.1997G>A
NG_055295.1:g.5882G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.172G>A	ENSP00000476098.1:p.Gly58Arg
ENST00000610963.1:c.171G>A	ENSP00000481371.1:p.Trp57Ter
ENST00000616270.4:c.172G>A	ENSP00000480679.1:p.Gly58Arg
ENST00000634680.1:c.151+454G>A	ENSP00000489240.1:n.151+454G>A
ENST00000634967.1:c.172G>A	ENSP00000489559.1:p.Gly58Arg
NR_074079.1:n.449G>A