Canonical Allele Identifier: CA507655483
Gene: IFNL4 HGNC NCBI

Linked Data

gnomAD v4: 19-39247446-T-G
MyVariant Identifiers: chr19:g.39738086T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247446T>G , CM000681.2:g.39247446T>G GRCh38
NC_000019.9:g.39738086T>G , CM000681.1:g.39738086T>G GRCh37
NC_000019.8:g.44429926T>G NCBI36
NG_042193.1:g.2526A>C
NG_055295.1:g.6411A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.385A>C ENSP00000476098.1:p.Arg129=
ENST00000610963.1:c.384A>C ENSP00000481371.1:p.Pro128=
ENST00000616270.4:c.422+22A>C ENSP00000480679.1:n.422+22A>C
ENST00000634680.1:c.169A>C ENSP00000489240.1:p.Arg57=
ENST00000634967.1:c.241A>C ENSP00000489559.1:p.Arg81=
NR_074079.1:n.662A>C
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