Canonical Allele Identifier: CA2335423560
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs2074954574
gnomAD v3: 19-39247548-T-C
gnomAD v4: 19-39247548-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247548T>C , CM000681.2:g.39247548T>C GRCh38
NC_000019.9:g.39738188T>C , CM000681.1:g.39738188T>C GRCh37
NC_000019.8:g.44430028T>C NCBI36
NG_042193.1:g.2424A>G
NG_055295.1:g.6309A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.368-85A>G ENSP00000476098.1:n.368-85A>G
ENST00000610963.1:c.367-85A>G ENSP00000481371.1:n.367-85A>G
ENST00000616270.4:c.342A>G ENSP00000480679.1:p.Arg114=
ENST00000634680.1:c.152-85A>G ENSP00000489240.1:n.152-85A>G
ENST00000634967.1:c.224-85A>G ENSP00000489559.1:n.224-85A>G
NR_074079.1:n.645-85A>G
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