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Canonical Allele Identifier:
CA9426137
Gene: IFNL4
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39247226C>G , CM000681.2:g.39247226C>G
GRCh38
NC_000019.9:g.39737866C>G , CM000681.1:g.39737866C>G
GRCh37
NC_000019.8:g.44429706C>G
NCBI36
NG_042193.1:g.2746G>C
NG_055295.1:g.6631G>C
Transcript Alleles
HGVS
Amino-acid Change
NR_074079.1:n.725G>C
ENST00000606380.2:c.448G>C
ENSP00000476098.1:p.Ala150Pro
ENST00000610963.1:c.447G>C
ENSP00000481371.1:p.Ser149=
ENST00000616270.4:c.422+242G>C
ENSP00000480679.1:n.422+242G>C
ENST00000634680.1:c.232G>C
ENSP00000489240.1:p.Ala78Pro
ENST00000634967.1:c.304G>C
ENSP00000489559.1:p.Ala102Pro
Search 100 bp 5'
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