Canonical Allele Identifier: CA405756692

Gene: IFNL4

Linked Data

• MyVariant Identifiers: chr19:g.39738586C>G (hg19) ; chr19:g.39247946C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247946C>G , CM000681.2:g.39247946C>G	GRCh38
NC_000019.9:g.39738586C>G , CM000681.1:g.39738586C>G	GRCh37
NC_000019.8:g.44430426C>G	NCBI36
NG_042193.1:g.2026G>C
NG_055295.1:g.5911G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.201G>C	ENSP00000476098.1:p.Gln67His
ENST00000610963.1:c.200G>C	ENSP00000481371.1:p.Arg67Thr
ENST00000616270.4:c.201G>C	ENSP00000480679.1:p.Gln67His
ENST00000634680.1:c.152-483G>C	ENSP00000489240.1:n.152-483G>C
ENST00000634967.1:c.201G>C	ENSP00000489559.1:p.Gln67His
NR_074079.1:n.478G>C