Canonical Allele Identifier: CA405756731

Gene: IFNL4

Linked Data

• dbSNP Id: rs1260045647
• gnomAD v3: 19-39247953-G-A
• gnomAD v4: 19-39247953-G-A
• MyVariant Identifiers: chr19:g.39738593G>A (hg19) ; chr19:g.39247953G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247953G>A , CM000681.2:g.39247953G>A	GRCh38
NC_000019.9:g.39738593G>A , CM000681.1:g.39738593G>A	GRCh37
NC_000019.8:g.44430433G>A	NCBI36
NG_042193.1:g.2019C>T
NG_055295.1:g.5904C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.194C>T	ENSP00000476098.1:p.Pro65Leu
ENST00000610963.1:c.193C>T	ENSP00000481371.1:p.Arg65Cys
ENST00000616270.4:c.194C>T	ENSP00000480679.1:p.Pro65Leu
ENST00000634680.1:c.151+476C>T	ENSP00000489240.1:n.151+476C>T
ENST00000634967.1:c.194C>T	ENSP00000489559.1:p.Pro65Leu
NR_074079.1:n.471C>T