Canonical Allele Identifier: CA2335422188

Gene: IFNL3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39244656G= , CM000681.2:g.39244656G=	GRCh38
NC_000019.9:g.39735296G= , CM000681.1:g.39735296G=	GRCh37
NC_000019.8:g.44427136G=	NCBI36
NG_042193.1:g.5316C=
NG_055295.1:g.9201C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.192+132C=	ENSP00000481633.1:n.192+132C=
ENST00000413851.3:c.180+132C= MANE Select	ENSP00000409000.2:n.180+132C=
ENST00000413851.2:c.180+132C=	ENSP00000409000.2:n.180+132C=
ENST00000613087.4:c.192+132C=	ENSP00000481633.1:n.192+132C=
NM_172139.2:c.180+132C=	NP_742151.2:n.180+132C=
XM_005258765.3:c.192+132C=	XP_005258822.1:n.192+132C=
XM_011526757.1:c.192+132C=	XP_011525059.1:n.192+132C=
NM_001346937.1:c.192+132C=	NP_001333866.1:n.192+132C=
NM_172139.3:c.180+132C=	NP_742151.2:n.180+132C=
NM_172139.4:c.180+132C= MANE Select	NP_742151.2:n.180+132C=
NM_001346937.2:c.192+132C=	NP_001333866.1:n.192+132C=