Canonical Allele Identifier: CA308218487
Gene: IFNL3 HGNC NCBI

Linked Data

dbSNP Id: rs199512141
gnomAD v4: 19-39243576-T-A
MyVariant Identifiers: chr19:g.39734216T>A (hg19) chr19:g.39243576T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243576T>A , CM000681.2:g.39243576T>A GRCh38
NC_000019.9:g.39734216T>A , CM000681.1:g.39734216T>A GRCh37
NC_000019.8:g.44426056T>A NCBI36
NG_042193.1:g.6396A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.*56A>T ENSP00000481633.1:n.*56A>T
ENST00000413851.3:c.*56A>T MANE Select ENSP00000409000.2:n.*56A>T
ENST00000613087.4:c.*56A>T ENSP00000481633.1:n.*56A>T
NM_172139.4:c.*56A>T MANE Select NP_742151.2:n.*56A>T
NM_001346937.2:c.*56A>T NP_001333866.1:n.*56A>T
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