Canonical Allele Identifier: CA882119608
Gene: IFNL4 HGNC NCBI

Linked Data

dbSNP Id: rs1178184496
MyVariant Identifiers: chr19:g.39738985A>C (hg19) chr19:g.39248345A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248345A>C , CM000681.2:g.39248345A>C GRCh38
NC_000019.9:g.39738985A>C , CM000681.1:g.39738985A>C GRCh37
NC_000019.8:g.44430825A>C NCBI36
NG_042193.1:g.1627T>G
NG_055295.1:g.5512T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.151+84T>G ENSP00000476098.1:n.151+84T>G
ENST00000610963.1:c.150+84T>G ENSP00000481371.1:n.150+84T>G
ENST00000616270.4:c.151+84T>G ENSP00000480679.1:n.151+84T>G
ENST00000634680.1:c.151+84T>G ENSP00000489240.1:n.151+84T>G
ENST00000634967.1:c.151+84T>G ENSP00000489559.1:n.151+84T>G
NR_074079.1:n.428+84T>G
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