Canonical Allele Identifier: CA308218429
Gene: IFNL3 HGNC NCBI

Linked Data

dbSNP Id: rs890082546
gnomAD v3: 19-39243510-A-T
gnomAD v4: 19-39243510-A-T
MyVariant Identifiers: chr19:g.39734150A>T (hg19) chr19:g.39243510A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243510A>T , CM000681.2:g.39243510A>T GRCh38
NC_000019.9:g.39734150A>T , CM000681.1:g.39734150A>T GRCh37
NC_000019.8:g.44425990A>T NCBI36
NG_042193.1:g.6462T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.*122T>A ENSP00000481633.1:n.*122T>A
NM_001346937.2:c.*122T>A NP_001333866.1:n.*122T>A
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