Canonical Allele Identifier: CA2576778125
Gene: IFNL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243583A>C , CM000681.2:g.39243583A>C GRCh38
NC_000019.9:g.39734223A>C , CM000681.1:g.39734223A>C GRCh37
NC_000019.8:g.44426063A>C NCBI36
NG_042193.1:g.6389T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000613087.5:c.*49T>G ENSP00000481633.1:n.*49T>G
ENST00000413851.3:c.*49T>G MANE Select ENSP00000409000.2:n.*49T>G
ENST00000613087.4:c.*49T>G ENSP00000481633.1:n.*49T>G
NM_172139.4:c.*49T>G MANE Select NP_742151.2:n.*49T>G
NM_001346937.2:c.*49T>G NP_001333866.1:n.*49T>G