Canonical Allele Identifier: CA2584993490
Gene: IFNL3 HGNC NCBI

Linked Data

gnomAD v4: 19-39243610-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243610G>T , CM000681.2:g.39243610G>T GRCh38
NC_000019.9:g.39734250G>T , CM000681.1:g.39734250G>T GRCh37
NC_000019.8:g.44426090G>T NCBI36
NG_042193.1:g.6362C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000613087.5:c.*22C>A ENSP00000481633.1:n.*22C>A
ENST00000413851.3:c.*22C>A MANE Select ENSP00000409000.2:n.*22C>A
ENST00000413851.2:c.*22C>A ENSP00000409000.2:n.*22C>A
ENST00000613087.4:c.*22C>A ENSP00000481633.1:n.*22C>A
XM_005258765.3:c.*22C>A XP_005258822.1:n.*22C>A
XM_011526757.1:c.*22C>A XP_011525059.1:n.*22C>A
NM_001346937.1:c.625C>A NP_001333866.1:n.625C>A
NM_172139.3:c.*22C>A NP_742151.2:n.*22C>A
NM_172139.4:c.*22C>A MANE Select NP_742151.2:n.*22C>A
NM_001346937.2:c.*22C>A NP_001333866.1:n.*22C>A
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