Canonical Allele Identifier: CA882119203

Gene: IFNL4

Linked Data

• dbSNP Id: rs1183518652
• gnomAD v3: 19-39247881-C-G
• gnomAD v4: 19-39247881-C-G
• MyVariant Identifiers: chr19:g.39738521C>G (hg19) ; chr19:g.39247881C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247881C>G , CM000681.2:g.39247881C>G	GRCh38
NC_000019.9:g.39738521C>G , CM000681.1:g.39738521C>G	GRCh37
NC_000019.8:g.44430361C>G	NCBI36
NG_042193.1:g.2091G>C
NG_055295.1:g.5976G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000606380.2:c.224-30G>C	ENSP00000476098.1:n.224-30G>C
ENST00000610963.1:c.223-30G>C	ENSP00000481371.1:n.223-30G>C
ENST00000616270.4:c.223+43G>C	ENSP00000480679.1:n.223+43G>C
ENST00000634680.1:c.152-418G>C	ENSP00000489240.1:n.152-418G>C
ENST00000634967.1:c.223+43G>C	ENSP00000489559.1:n.223+43G>C
NR_074079.1:n.501-30G>C