Canonical Allele Identifier: CA9426147
Gene: IFNL4 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.39248489C>G
GRCh37 chr19:g.39739129C>G
gnomAD v2:
19:39739129 C / G
gnomAD v3:
19:39248489 C / G
gnomAD v4:
chr19-39248489-C-G
Joint Max Group AF 0.2838303 (AMR)
Genomes Max Group AF 0.27175573 (AMR)
Exomes Max Group AF 0.29922508 (AMR)
dbSNP:
4803221
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39248489C>G , CM000681.2:g.39248489C>G GRCh38
NC_000019.9:g.39739129C>G , CM000681.1:g.39739129C>G GRCh37
NC_000019.8:g.44430969C>G NCBI36
NG_042193.1:g.1483G>C
NG_055295.1:g.5368G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000606380.2:c.91G>C ENSP00000476098.1:p.Ala31Pro
ENST00000610963.1:c.90G>C ENSP00000481371.1:p.Ser30=
ENST00000616270.4:c.91G>C ENSP00000480679.1:p.Ala31Pro
ENST00000634680.1:c.91G>C ENSP00000489240.1:p.Ala31Pro
ENST00000634967.1:c.91G>C ENSP00000489559.1:p.Ala31Pro
NR_074079.1:n.368G>C
Search 100 bp 5'
Search 100 bp 3'