Canonical Allele Identifier: CA1221566175

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437419G= , CM000663.2:g.218437419G=	GRCh38
NC_000001.10:g.218610761G= , CM000663.1:g.218610761G=	GRCh37
NC_000001.9:g.216677384G=	NCBI36
NG_027721.1:g.97086G=
NG_027721.2:g.97086G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1009G= MANE Select	ENSP00000355897.4:p.Glu337=
ENST00000366929.4:c.1093G=	ENSP00000355896.4:p.Glu365=
ENST00000366930.8:c.1009G=	ENSP00000355897.4:p.Glu337=
ENST00000479322.1:n.493G=
NM_001135599.2:c.1093G=	NP_001129071.1:p.Glu365=
NM_003238.3:c.1009G=	NP_003229.1:p.Glu337=
NM_001135599.3:c.1093G=	NP_001129071.1:p.Glu365=
NM_003238.4:c.1009G=	NP_003229.1:p.Glu337=
NR_138148.1:n.2312G=
NR_138149.1:n.2396G=
NM_003238.5:c.1009G=	NP_003229.1:p.Glu337=
NM_003238.6:c.1009G= MANE Select	NP_003229.1:p.Glu337=
NM_001135599.4:c.1093G=	NP_001129071.1:p.Glu365=
NR_138148.2:n.2260G=
NR_138149.2:n.2344G=