Canonical Allele Identifier: CA9426137
Gene: IFNL4 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.39247226C>G
GRCh37 chr19:g.39737866C>G
gnomAD v2:
19:39737866 C / G
gnomAD v3:
19:39247226 C / G
gnomAD v4:
chr19-39247226-C-G
Joint Max Group AF 0.28391234 (AMR)
Genomes Max Group AF 0.27139675 (AMR)
Exomes Max Group AF 0.30016058 (AMR)
dbSNP:
12971396
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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
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
NR_074079.1:n.725G>C
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