Canonical Allele Identifier: CA2335421527

Gene: IFNL3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39243606C= , CM000681.2:g.39243606C=	GRCh38
NC_000019.9:g.39734246C= , CM000681.1:g.39734246C=	GRCh37
NC_000019.8:g.44426086C=	NCBI36
NG_042193.1:g.6366G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000613087.5:c.*26G=	ENSP00000481633.1:n.*26G=
ENST00000413851.3:c.*26G= MANE Select	ENSP00000409000.2:n.*26G=
ENST00000413851.2:c.*26G=	ENSP00000409000.2:n.*26G=
ENST00000613087.4:c.*26G=	ENSP00000481633.1:n.*26G=
XM_005258765.3:c.*26G=	XP_005258822.1:n.*26G=
XM_011526757.1:c.*26G=	XP_011525059.1:n.*26G=
NM_001346937.1:c.629G=	NP_001333866.1:n.629G=
NM_172139.3:c.*26G=	NP_742151.2:n.*26G=
NM_172139.4:c.*26G= MANE Select	NP_742151.2:n.*26G=
NM_001346937.2:c.*26G=	NP_001333866.1:n.*26G=