Canonical Allele Identifier: CA2335423645
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs541447480

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247694C>G , CM000681.2:g.39247694C>G GRCh38
NC_000019.9:g.39738334C>G , CM000681.1:g.39738334C>G GRCh37
NC_000019.8:g.44430174C>G NCBI36
NG_042193.1:g.2278G>C
NG_055295.1:g.6163G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.367+14G>C ENSP00000476098.1:n.367+14G>C
ENST00000610963.1:c.366+14G>C ENSP00000481371.1:n.366+14G>C
ENST00000616270.4:c.224-28G>C ENSP00000480679.1:n.224-28G>C
ENST00000634680.1:c.152-231G>C ENSP00000489240.1:n.152-231G>C
ENST00000634967.1:c.224-231G>C ENSP00000489559.1:n.224-231G>C
NR_074079.1:n.644+14G>C