Canonical Allele Identifier: CA2335422082

Gene: IFNL3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244490T= , CM000681.2:g.39244490T=	GRCh38
NC_000019.9:g.39735130T= , CM000681.1:g.39735130T=	GRCh37
NC_000019.8:g.44426970T=	NCBI36
NG_042193.1:g.5482A=
NG_055295.1:g.9367A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.197A=	ENSP00000481633.1:p.Glu66=
ENST00000413851.3:c.185A= MANE Select	ENSP00000409000.2:p.Glu62=
ENST00000413851.2:c.185A=	ENSP00000409000.2:p.Glu62=
ENST00000613087.4:c.197A=	ENSP00000481633.1:p.Glu66=
NM_172139.2:c.185A=	NP_742151.2:p.Glu62=
XM_005258765.3:c.197A=	XP_005258822.1:p.Glu66=
XM_011526757.1:c.197A=	XP_011525059.1:p.Glu66=
NM_001346937.1:c.197A=	NP_001333866.1:p.Glu66=
NM_172139.3:c.185A=	NP_742151.2:p.Glu62=
NM_172139.4:c.185A= MANE Select	NP_742151.2:p.Glu62=
NM_001346937.2:c.197A=	NP_001333866.1:p.Glu66=