Canonical Allele Identifier: CA2504727494
Gene: IFNL4 HGNC NCBI

Linked Data

gnomAD v4: 19-39248350-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248350C>A , CM000681.2:g.39248350C>A GRCh38
NC_000019.9:g.39738990C>A , CM000681.1:g.39738990C>A GRCh37
NC_000019.8:g.44430830C>A NCBI36
NG_042193.1:g.1622G>T
NG_055295.1:g.5507G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.151+79G>T ENSP00000476098.1:n.151+79G>T
ENST00000610963.1:c.150+79G>T ENSP00000481371.1:n.150+79G>T
ENST00000616270.4:c.151+79G>T ENSP00000480679.1:n.151+79G>T
ENST00000634680.1:c.151+79G>T ENSP00000489240.1:n.151+79G>T
ENST00000634967.1:c.151+79G>T ENSP00000489559.1:n.151+79G>T
NR_074079.1:n.428+79G>T
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