Canonical Allele Identifier: CA882115765
Gene: IFNL3 HGNC NCBI

Linked Data

dbSNP Id: rs1336132194
gnomAD v4: 19-39243553-A-G
MyVariant Identifiers: chr19:g.39734193A>G (hg19) chr19:g.39243553A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243553A>G , CM000681.2:g.39243553A>G GRCh38
NC_000019.9:g.39734193A>G , CM000681.1:g.39734193A>G GRCh37
NC_000019.8:g.44426033A>G NCBI36
NG_042193.1:g.6419T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.*79T>C ENSP00000481633.1:n.*79T>C
ENST00000413851.3:c.*79T>C MANE Select ENSP00000409000.2:n.*79T>C
ENST00000613087.4:c.*79T>C ENSP00000481633.1:n.*79T>C
NM_172139.4:c.*79T>C MANE Select NP_742151.2:n.*79T>C
NM_001346937.2:c.*79T>C NP_001333866.1:n.*79T>C
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