Canonical Allele Identifier: CA308189517

Gene: IFNL4

Linked Data

• dbSNP Id: rs529794067
• gnomAD v2: 19-39738618-G-T
• gnomAD v3: 19-39247978-G-T
• gnomAD v4: 19-39247978-G-T
• COSMIC: COSN1215453
• MyVariant Identifiers: chr19:g.39738618G>T (hg19) ; chr19:g.39247978G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247978G>T , CM000681.2:g.39247978G>T	GRCh38
NC_000019.9:g.39738618G>T , CM000681.1:g.39738618G>T	GRCh37
NC_000019.8:g.44430458G>T	NCBI36
NG_042193.1:g.1994C>A
NG_055295.1:g.5879C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.169C>A	ENSP00000476098.1:p.Leu57Met
ENST00000610963.1:c.168C>A	ENSP00000481371.1:p.Ser56Arg
ENST00000616270.4:c.169C>A	ENSP00000480679.1:p.Leu57Met
ENST00000634680.1:c.151+451C>A	ENSP00000489240.1:n.151+451C>A
ENST00000634967.1:c.169C>A	ENSP00000489559.1:p.Leu57Met
NR_074079.1:n.446C>A