Canonical Allele Identifier: CA882119417
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs749352830

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248024C>G , CM000681.2:g.39248024C>G GRCh38
NC_000019.9:g.39738664C>G , CM000681.1:g.39738664C>G GRCh37
NC_000019.8:g.44430504C>G NCBI36
NG_042193.1:g.1948G>C
NG_055295.1:g.5833G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-29G>C ENSP00000476098.1:n.152-29G>C
ENST00000610963.1:c.151-29G>C ENSP00000481371.1:n.151-29G>C
ENST00000616270.4:c.152-29G>C ENSP00000480679.1:n.152-29G>C
ENST00000634680.1:c.151+405G>C ENSP00000489240.1:n.151+405G>C
ENST00000634967.1:c.152-29G>C ENSP00000489559.1:n.152-29G>C
NR_074079.1:n.429-29G>C