Canonical Allele Identifier: CA507655493

Gene: IFNL4

Linked Data

• dbSNP Id: rs1182069665
• gnomAD v4: 19-39247452-T-C
• MyVariant Identifiers: chr19:g.39738092T>C (hg19) ; chr19:g.39247452T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39247452T>C , CM000681.2:g.39247452T>C	GRCh38
NC_000019.9:g.39738092T>C , CM000681.1:g.39738092T>C	GRCh37
NC_000019.8:g.44429932T>C	NCBI36
NG_042193.1:g.2520A>G
NG_055295.1:g.6405A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000606380.2:c.379A>G	ENSP00000476098.1:p.Thr127Ala
ENST00000610963.1:c.378A>G	ENSP00000481371.1:p.Ala126=
ENST00000616270.4:c.422+16A>G	ENSP00000480679.1:n.422+16A>G
ENST00000634680.1:c.163A>G	ENSP00000489240.1:p.Thr55Ala
ENST00000634967.1:c.235A>G	ENSP00000489559.1:p.Thr79Ala
NR_074079.1:n.656A>G