Canonical Allele Identifier: CA2584995002
Gene: IFNL4 HGNC NCBI

Linked Data

gnomAD v4: 19-39248278-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248278G>T , CM000681.2:g.39248278G>T GRCh38
NC_000019.9:g.39738918G>T , CM000681.1:g.39738918G>T GRCh37
NC_000019.8:g.44430758G>T NCBI36
NG_042193.1:g.1694C>A
NG_055295.1:g.5579C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.151+151C>A ENSP00000476098.1:n.151+151C>A
ENST00000610963.1:c.150+151C>A ENSP00000481371.1:n.150+151C>A
ENST00000616270.4:c.151+151C>A ENSP00000480679.1:n.151+151C>A
ENST00000634680.1:c.151+151C>A ENSP00000489240.1:n.151+151C>A
ENST00000634967.1:c.151+151C>A ENSP00000489559.1:n.151+151C>A
NR_074079.1:n.428+151C>A
Search 100 bp 5'
Search 100 bp 3'