Canonical Allele Identifier: CA405756052

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738367C>G (hg19) ; chr19:g.39247727C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247727C>G , CM000681.2:g.39247727C>G	GRCh38
NC_000019.9:g.39738367C>G , CM000681.1:g.39738367C>G	GRCh37
NC_000019.8:g.44430207C>G	NCBI36
NG_042193.1:g.2245G>C
NG_055295.1:g.6130G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.348G>C	ENSP00000476098.1:p.Gly116=
ENST00000610963.1:c.347G>C	ENSP00000481371.1:p.Gly116Ala
ENST00000616270.4:c.224-61G>C	ENSP00000480679.1:n.224-61G>C
ENST00000634680.1:c.152-264G>C	ENSP00000489240.1:n.152-264G>C
ENST00000634967.1:c.223+197G>C	ENSP00000489559.1:n.223+197G>C
NR_074079.1:n.625G>C