Canonical Allele Identifier: CA882119427
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs1174792662

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248031G>A , CM000681.2:g.39248031G>A GRCh38
NC_000019.9:g.39738671G>A , CM000681.1:g.39738671G>A GRCh37
NC_000019.8:g.44430511G>A NCBI36
NG_042193.1:g.1941C>T
NG_055295.1:g.5826C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-36C>T ENSP00000476098.1:n.152-36C>T
ENST00000610963.1:c.151-36C>T ENSP00000481371.1:n.151-36C>T
ENST00000616270.4:c.152-36C>T ENSP00000480679.1:n.152-36C>T
ENST00000634680.1:c.151+398C>T ENSP00000489240.1:n.151+398C>T
ENST00000634967.1:c.152-36C>T ENSP00000489559.1:n.152-36C>T
NR_074079.1:n.429-36C>T