Canonical Allele Identifier: CA2576778121
Gene: IFNL3 HGNC NCBI

Linked Data

gnomAD v4: 19-39243571-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243571T>C , CM000681.2:g.39243571T>C GRCh38
NC_000019.9:g.39734211T>C , CM000681.1:g.39734211T>C GRCh37
NC_000019.8:g.44426051T>C NCBI36
NG_042193.1:g.6401A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.*61A>G ENSP00000481633.1:n.*61A>G
ENST00000413851.3:c.*61A>G MANE Select ENSP00000409000.2:n.*61A>G
ENST00000613087.4:c.*61A>G ENSP00000481633.1:n.*61A>G
NM_172139.4:c.*61A>G MANE Select NP_742151.2:n.*61A>G
NM_001346937.2:c.*61A>G NP_001333866.1:n.*61A>G
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