Canonical Allele Identifier: CA308189607
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs181637919

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248103G>C , CM000681.2:g.39248103G>C GRCh38
NC_000019.9:g.39738743G>C , CM000681.1:g.39738743G>C GRCh37
NC_000019.8:g.44430583G>C NCBI36
NG_042193.1:g.1869C>G
NG_055295.1:g.5754C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-108C>G ENSP00000476098.1:n.152-108C>G
ENST00000610963.1:c.151-108C>G ENSP00000481371.1:n.151-108C>G
ENST00000616270.4:c.152-108C>G ENSP00000480679.1:n.152-108C>G
ENST00000634680.1:c.151+326C>G ENSP00000489240.1:n.151+326C>G
ENST00000634967.1:c.152-108C>G ENSP00000489559.1:n.152-108C>G
NR_074079.1:n.429-108C>G