Canonical Allele Identifier: CA405755989

Gene: IFNL4

Linked Data

• dbSNP Id: rs2144976126
• MyVariant Identifiers: chr19:g.39738352G>C (hg19) ; chr19:g.39247712G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247712G>C , CM000681.2:g.39247712G>C	GRCh38
NC_000019.9:g.39738352G>C , CM000681.1:g.39738352G>C	GRCh37
NC_000019.8:g.44430192G>C	NCBI36
NG_042193.1:g.2260C>G
NG_055295.1:g.6145C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.363C>G	ENSP00000476098.1:p.Gly121=
ENST00000610963.1:c.362C>G	ENSP00000481371.1:p.Ala121Gly
ENST00000616270.4:c.224-46C>G	ENSP00000480679.1:n.224-46C>G
ENST00000634680.1:c.152-249C>G	ENSP00000489240.1:n.152-249C>G
ENST00000634967.1:c.223+212C>G	ENSP00000489559.1:n.223+212C>G
NR_074079.1:n.640C>G