Canonical Allele Identifier: CA405756473

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738472T>C (hg19) ; chr19:g.39247832T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247832T>C , CM000681.2:g.39247832T>C	GRCh38
NC_000019.9:g.39738472T>C , CM000681.1:g.39738472T>C	GRCh37
NC_000019.8:g.44430312T>C	NCBI36
NG_042193.1:g.2140A>G
NG_055295.1:g.6025A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.243A>G	ENSP00000476098.1:p.Pro81=
ENST00000610963.1:c.242A>G	ENSP00000481371.1:p.His81Arg
ENST00000616270.4:c.223+92A>G	ENSP00000480679.1:n.223+92A>G
ENST00000634680.1:c.152-369A>G	ENSP00000489240.1:n.152-369A>G
ENST00000634967.1:c.223+92A>G	ENSP00000489559.1:n.223+92A>G
NR_074079.1:n.520A>G