Canonical Allele Identifier: CA507407705

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738471G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247831G>A , CM000681.2:g.39247831G>A	GRCh38
NC_000019.9:g.39738471G>A , CM000681.1:g.39738471G>A	GRCh37
NC_000019.8:g.44430311G>A	NCBI36
NG_042193.1:g.2141C>T
NG_055295.1:g.6026C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.244C>T	ENSP00000476098.1:p.Arg82Cys
ENST00000610963.1:c.243C>T	ENSP00000481371.1:p.His81=
ENST00000616270.4:c.223+93C>T	ENSP00000480679.1:n.223+93C>T
ENST00000634680.1:c.152-368C>T	ENSP00000489240.1:n.152-368C>T
ENST00000634967.1:c.223+93C>T	ENSP00000489559.1:n.223+93C>T
NR_074079.1:n.521C>T