Canonical Allele Identifier: CA882119228
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs1241424035
gnomAD v4: 19-39247903-C-T
MyVariant Identifiers: chr19:g.39738543C>T (hg19) chr19:g.39247903C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247903C>T , CM000681.2:g.39247903C>T GRCh38
NC_000019.9:g.39738543C>T , CM000681.1:g.39738543C>T GRCh37
NC_000019.8:g.44430383C>T NCBI36
NG_042193.1:g.2069G>A
NG_055295.1:g.5954G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000606380.2:c.223+21G>A ENSP00000476098.1:n.223+21G>A
ENST00000610963.1:c.222+21G>A ENSP00000481371.1:n.222+21G>A
ENST00000616270.4:c.223+21G>A ENSP00000480679.1:n.223+21G>A
ENST00000634680.1:c.152-440G>A ENSP00000489240.1:n.152-440G>A
ENST00000634967.1:c.223+21G>A ENSP00000489559.1:n.223+21G>A
NR_074079.1:n.500+21G>A
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