Canonical Allele Identifier: CA2584993496
Gene: IFNL3 HGNC NCBI

Linked Data

gnomAD v4: 19-39243617-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243617T>C , CM000681.2:g.39243617T>C GRCh38
NC_000019.9:g.39734257T>C , CM000681.1:g.39734257T>C GRCh37
NC_000019.8:g.44426097T>C NCBI36
NG_042193.1:g.6355A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000613087.5:c.*15A>G ENSP00000481633.1:n.*15A>G
ENST00000413851.3:c.*15A>G MANE Select ENSP00000409000.2:n.*15A>G
ENST00000413851.2:c.*15A>G ENSP00000409000.2:n.*15A>G
ENST00000613087.4:c.*15A>G ENSP00000481633.1:n.*15A>G
XM_005258765.3:c.*15A>G XP_005258822.1:n.*15A>G
XM_011526757.1:c.*15A>G XP_011525059.1:n.*15A>G
NM_001346937.1:c.618A>G NP_001333866.1:n.618A>G
NM_172139.3:c.*15A>G NP_742151.2:n.*15A>G
NM_172139.4:c.*15A>G MANE Select NP_742151.2:n.*15A>G
NM_001346937.2:c.*15A>G NP_001333866.1:n.*15A>G
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