Canonical Allele Identifier: CA633069320
Gene: IFNL4 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248055T>G , CM000681.2:g.39248055T>G GRCh38
NC_000019.9:g.39738695T>G , CM000681.1:g.39738695T>G GRCh37
NC_000019.8:g.44430535T>G NCBI36
NG_042193.1:g.1917A>C
NG_055295.1:g.5802A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.152-60A>C ENSP00000476098.1:n.152-60A>C
ENST00000610963.1:c.151-60A>C ENSP00000481371.1:n.151-60A>C
ENST00000616270.4:c.152-60A>C ENSP00000480679.1:n.152-60A>C
ENST00000634680.1:c.151+374A>C ENSP00000489240.1:n.151+374A>C
ENST00000634967.1:c.152-60A>C ENSP00000489559.1:n.152-60A>C
NR_074079.1:n.429-60A>C