Canonical Allele Identifier: CA2335423874
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs2074957984

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248129G>C , CM000681.2:g.39248129G>C GRCh38
NC_000019.9:g.39738769G>C , CM000681.1:g.39738769G>C GRCh37
NC_000019.8:g.44430609G>C NCBI36
NG_042193.1:g.1843C>G
NG_055295.1:g.5728C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-134C>G ENSP00000476098.1:n.152-134C>G
ENST00000610963.1:c.151-134C>G ENSP00000481371.1:n.151-134C>G
ENST00000616270.4:c.152-134C>G ENSP00000480679.1:n.152-134C>G
ENST00000634680.1:c.151+300C>G ENSP00000489240.1:n.151+300C>G
ENST00000634967.1:c.152-134C>G ENSP00000489559.1:n.152-134C>G
NR_074079.1:n.429-134C>G