Canonical Allele Identifier: CA405756749

Gene: IFNL4

Linked Data

• dbSNP Id: rs1210849664
• gnomAD v3: 19-39247956-A-C
• gnomAD v4: 19-39247956-A-C
• MyVariant Identifiers: chr19:g.39738596A>C (hg19) ; chr19:g.39247956A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247956A>C , CM000681.2:g.39247956A>C	GRCh38
NC_000019.9:g.39738596A>C , CM000681.1:g.39738596A>C	GRCh37
NC_000019.8:g.44430436A>C	NCBI36
NG_042193.1:g.2016T>G
NG_055295.1:g.5901T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.191T>G	ENSP00000476098.1:p.Leu64Arg
ENST00000610963.1:c.190T>G	ENSP00000481371.1:p.Phe64Val
ENST00000616270.4:c.191T>G	ENSP00000480679.1:p.Leu64Arg
ENST00000634680.1:c.151+473T>G	ENSP00000489240.1:n.151+473T>G
ENST00000634967.1:c.191T>G	ENSP00000489559.1:p.Leu64Arg
NR_074079.1:n.468T>G