Canonical Allele Identifier: CA2335422192

Gene: IFNL3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244659G= , CM000681.2:g.39244659G=	GRCh38
NC_000019.9:g.39735299G= , CM000681.1:g.39735299G=	GRCh37
NC_000019.8:g.44427139G=	NCBI36
NG_042193.1:g.5313C=
NG_055295.1:g.9198C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.192+129C=	ENSP00000481633.1:n.192+129C=
ENST00000413851.3:c.180+129C= MANE Select	ENSP00000409000.2:n.180+129C=
ENST00000413851.2:c.180+129C=	ENSP00000409000.2:n.180+129C=
ENST00000613087.4:c.192+129C=	ENSP00000481633.1:n.192+129C=
NM_172139.2:c.180+129C=	NP_742151.2:n.180+129C=
XM_005258765.3:c.192+129C=	XP_005258822.1:n.192+129C=
XM_011526757.1:c.192+129C=	XP_011525059.1:n.192+129C=
NM_001346937.1:c.192+129C=	NP_001333866.1:n.192+129C=
NM_172139.3:c.180+129C=	NP_742151.2:n.180+129C=
NM_172139.4:c.180+129C= MANE Select	NP_742151.2:n.180+129C=
NM_001346937.2:c.192+129C=	NP_001333866.1:n.192+129C=