Canonical Allele Identifier: CA405756911

Gene: IFNL4

Linked Data

• gnomAD v4: 19-39247986-C-T
• MyVariant Identifiers: chr19:g.39738626C>T (hg19) ; chr19:g.39247986C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247986C>T , CM000681.2:g.39247986C>T	GRCh38
NC_000019.9:g.39738626C>T , CM000681.1:g.39738626C>T	GRCh37
NC_000019.8:g.44430466C>T	NCBI36
NG_042193.1:g.1986G>A
NG_055295.1:g.5871G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.161G>A	ENSP00000476098.1:p.Gly54Asp
ENST00000610963.1:c.160G>A	ENSP00000481371.1:p.Ala54Thr
ENST00000616270.4:c.161G>A	ENSP00000480679.1:p.Gly54Asp
ENST00000634680.1:c.151+443G>A	ENSP00000489240.1:n.151+443G>A
ENST00000634967.1:c.161G>A	ENSP00000489559.1:p.Gly54Asp
NR_074079.1:n.438G>A