Canonical Allele Identifier: CA308218444
Gene: IFNL3 HGNC NCBI

Linked Data

dbSNP Id: rs112990542
gnomAD v2: 19-39734177-A-G
gnomAD v3: 19-39243537-A-G
gnomAD v4: 19-39243537-A-G
MyVariant Identifiers: chr19:g.39734177A>G (hg19) chr19:g.39243537A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243537A>G , CM000681.2:g.39243537A>G GRCh38
NC_000019.9:g.39734177A>G , CM000681.1:g.39734177A>G GRCh37
NC_000019.8:g.44426017A>G NCBI36
NG_042193.1:g.6435T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.*95T>C ENSP00000481633.1:n.*95T>C
NM_001346937.2:c.*95T>C NP_001333866.1:n.*95T>C
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