Canonical Allele Identifier: CA2335421552

Gene: IFNL3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39243649C= , CM000681.2:g.39243649C=	GRCh38
NC_000019.9:g.39734289C= , CM000681.1:g.39734289C=	GRCh37
NC_000019.8:g.44426129C=	NCBI36
NG_042193.1:g.6323G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613087.5:c.586G=	ENSP00000481633.1:p.Gly196=
ENST00000413851.3:c.574G= MANE Select	ENSP00000409000.2:p.Gly192=
ENST00000413851.2:c.574G=	ENSP00000409000.2:p.Gly192=
ENST00000613087.4:c.586G=	ENSP00000481633.1:p.Gly196=
NM_172139.2:c.574G=	NP_742151.2:p.Gly192=
XM_005258765.3:c.586G=	XP_005258822.1:p.Gly196=
XM_011526757.1:c.586G=	XP_011525059.1:p.Gly196=
NM_001346937.1:c.586G=	NP_001333866.1:p.Gly196=
NM_172139.3:c.574G=	NP_742151.2:p.Gly192=
NM_172139.4:c.574G= MANE Select	NP_742151.2:p.Gly192=
NM_001346937.2:c.586G=	NP_001333866.1:p.Gly196=