Canonical Allele Identifier: CA308189531
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs929035434

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248018C>G , CM000681.2:g.39248018C>G GRCh38
NC_000019.9:g.39738658C>G , CM000681.1:g.39738658C>G GRCh37
NC_000019.8:g.44430498C>G NCBI36
NG_042193.1:g.1954G>C
NG_055295.1:g.5839G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.152-23G>C ENSP00000476098.1:n.152-23G>C
ENST00000610963.1:c.151-23G>C ENSP00000481371.1:n.151-23G>C
ENST00000616270.4:c.152-23G>C ENSP00000480679.1:n.152-23G>C
ENST00000634680.1:c.151+411G>C ENSP00000489240.1:n.151+411G>C
ENST00000634967.1:c.152-23G>C ENSP00000489559.1:n.152-23G>C
NR_074079.1:n.429-23G>C