Canonical Allele Identifier: CA2335421521
Gene: IFNL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39243581C= , CM000681.2:g.39243581C= GRCh38
NC_000019.9:g.39734221C= , CM000681.1:g.39734221C= GRCh37
NC_000019.8:g.44426061C= NCBI36
NG_042193.1:g.6391G=

Transcript Alleles

HGVS Amino-acid change
ENST00000613087.5:c.*51G= ENSP00000481633.1:n.*51G=
ENST00000413851.3:c.*51G= MANE Select ENSP00000409000.2:n.*51G=
ENST00000613087.4:c.*51G= ENSP00000481633.1:n.*51G=
NM_172139.4:c.*51G= MANE Select NP_742151.2:n.*51G=
NM_001346937.2:c.*51G= NP_001333866.1:n.*51G=