Canonical Allele Identifier: CA1221555879

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405280G= , CM000663.2:g.218405280G=	GRCh38
NC_000001.10:g.218578622G= , CM000663.1:g.218578622G=	GRCh37
NC_000001.9:g.216645245G=	NCBI36
NG_027721.1:g.64947G=
NG_027721.2:g.64947G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003238.6:c.458G= MANE Select	NP_003229.1:p.Arg153=
ENST00000366930.9:c.458G= MANE Select	ENSP00000355897.4:p.Arg153=
NM_001135599.2:c.542G=	NP_001129071.1:p.Arg181=
NM_001135599.3:c.542G=	NP_001129071.1:p.Arg181=
NM_001135599.4:c.542G=	NP_001129071.1:p.Arg181=
NM_003238.3:c.458G=	NP_003229.1:p.Arg153=
NM_003238.4:c.458G=	NP_003229.1:p.Arg153=
NM_003238.5:c.458G=	NP_003229.1:p.Arg153=
NR_138148.1:n.1876G=
NR_138148.2:n.1824G=
NR_138149.1:n.1960G=
NR_138149.2:n.1908G=
ENST00000366929.4:c.542G=	ENSP00000355896.4:p.Arg181=
ENST00000366930.8:c.458G=	ENSP00000355897.4:p.Arg153=
ENST00000488793.1:n.122G=