Canonical Allele Identifier: CA507407723
Gene: IFNL4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.39738477G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39247837G>C , CM000681.2:g.39247837G>C GRCh38
NC_000019.9:g.39738477G>C , CM000681.1:g.39738477G>C GRCh37
NC_000019.8:g.44430317G>C NCBI36
NG_042193.1:g.2135C>G
NG_055295.1:g.6020C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.238C>G ENSP00000476098.1:p.Pro80Ala
ENST00000610963.1:c.237C>G ENSP00000481371.1:p.Leu79=
ENST00000616270.4:c.223+87C>G ENSP00000480679.1:n.223+87C>G
ENST00000634680.1:c.152-374C>G ENSP00000489240.1:n.152-374C>G
ENST00000634967.1:c.223+87C>G ENSP00000489559.1:n.223+87C>G
NR_074079.1:n.515C>G