ClinGen Allele Registry
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Canonical Allele Identifier:
CA507655561
Gene: IFNL4
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247226C>T , CM000681.2:g.39247226C>T
GRCh38
NC_000019.9:g.39737866C>T , CM000681.1:g.39737866C>T
GRCh37
NC_000019.8:g.44429706C>T
NCBI36
NG_042193.1:g.2746G>A
NG_055295.1:g.6631G>A
Transcript Alleles
HGVS
Amino-acid Change
NR_074079.1:n.725G>A
ENST00000606380.2:c.448G>A
ENSP00000476098.1:p.Ala150Thr
ENST00000610963.1:c.447G>A
ENSP00000481371.1:p.Ser149=
ENST00000616270.4:c.422+242G>A
ENSP00000480679.1:n.422+242G>A
ENST00000634680.1:c.232G>A
ENSP00000489240.1:p.Ala78Thr
ENST00000634967.1:c.304G>A
ENSP00000489559.1:p.Ala102Thr
Search 100 bp 5'
Search 100 bp 3'