Canonical Allele Identifier: CA882119455
Community Standard Title: NC_000019.10:g.39248100C>G
Gene: IFNL4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248100C>G , CM000681.2:g.39248100C>G GRCh38
NC_000019.9:g.39738740C>G , CM000681.1:g.39738740C>G GRCh37
NC_000019.8:g.44430580C>G NCBI36
NG_042193.1:g.1872G>C
NG_055295.1:g.5757G>C

Transcript Alleles

HGVS Amino-acid Change
NR_074079.1:n.429-105G>C
ENST00000606380.2:c.152-105G>C ENSP00000476098.1:n.152-105G>C
ENST00000610963.1:c.151-105G>C ENSP00000481371.1:n.151-105G>C
ENST00000616270.4:c.152-105G>C ENSP00000480679.1:n.152-105G>C
ENST00000634680.1:c.151+329G>C ENSP00000489240.1:n.151+329G>C
ENST00000634967.1:c.152-105G>C ENSP00000489559.1:n.152-105G>C
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