Canonical Allele Identifier: CA1221563187

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218434154G= , CM000663.2:g.218434154G=	GRCh38
NC_000001.10:g.218607496G= , CM000663.1:g.218607496G=	GRCh37
NC_000001.9:g.216674119G=	NCBI36
NG_027721.1:g.93821G=
NG_027721.2:g.93821G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003238.6:c.583G= MANE Select	NP_003229.1:p.Glu195=
ENST00000366930.9:c.583G= MANE Select	ENSP00000355897.4:p.Glu195=
NM_001135599.2:c.667G=	NP_001129071.1:p.Glu223=
NM_001135599.3:c.667G=	NP_001129071.1:p.Glu223=
NM_001135599.4:c.667G=	NP_001129071.1:p.Glu223=
NM_003238.3:c.583G=	NP_003229.1:p.Glu195=
NM_003238.4:c.583G=	NP_003229.1:p.Glu195=
NM_003238.5:c.583G=	NP_003229.1:p.Glu195=
NR_138148.1:n.2001G=
NR_138148.2:n.1949G=
NR_138149.1:n.2085G=
NR_138149.2:n.2033G=
ENST00000366929.4:c.667G=	ENSP00000355896.4:p.Glu223=
ENST00000366930.8:c.583G=	ENSP00000355897.4:p.Glu195=
ENST00000479322.1:n.29G=
ENST00000488793.1:n.247G=