Canonical Allele Identifier: CA405756728

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738592C>G (hg19) ; chr19:g.39247952C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247952C>G , CM000681.2:g.39247952C>G	GRCh38
NC_000019.9:g.39738592C>G , CM000681.1:g.39738592C>G	GRCh37
NC_000019.8:g.44430432C>G	NCBI36
NG_042193.1:g.2020G>C
NG_055295.1:g.5905G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.195G>C	ENSP00000476098.1:p.Pro65=
ENST00000610963.1:c.194G>C	ENSP00000481371.1:p.Arg65Pro
ENST00000616270.4:c.195G>C	ENSP00000480679.1:p.Pro65=
ENST00000634680.1:c.151+477G>C	ENSP00000489240.1:n.151+477G>C
ENST00000634967.1:c.195G>C	ENSP00000489559.1:p.Pro65=
NR_074079.1:n.472G>C