Canonical Allele Identifier: CA1221528655

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346802G= , CM000663.2:g.218346802G=	GRCh38
NC_000001.10:g.218520144G= , CM000663.1:g.218520144G=	GRCh37
NC_000001.9:g.216586767G=	NCBI36
NG_027721.1:g.6469G=
NG_027721.2:g.6469G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.101G= MANE Select	ENSP00000355897.4:p.Arg34=
ENST00000366929.4:c.101G=	ENSP00000355896.4:p.Arg34=
ENST00000366930.8:c.101G=	ENSP00000355897.4:p.Arg34=
NM_001135599.2:c.101G=	NP_001129071.1:p.Arg34=
NM_003238.3:c.101G=	NP_003229.1:p.Arg34=
NM_001135599.3:c.101G=	NP_001129071.1:p.Arg34=
NM_003238.4:c.101G=	NP_003229.1:p.Arg34=
NR_138148.1:n.1519G=
NR_138149.1:n.1519G=
NM_003238.5:c.101G=	NP_003229.1:p.Arg34=
NM_003238.6:c.101G= MANE Select	NP_003229.1:p.Arg34=
NM_001135599.4:c.101G=	NP_001129071.1:p.Arg34=
NR_138148.2:n.1467G=
NR_138149.2:n.1467G=