Canonical Allele Identifier: CA1221555718

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405082G= , CM000663.2:g.218405082G=	GRCh38
NC_000001.10:g.218578424G= , CM000663.1:g.218578424G=	GRCh37
NC_000001.9:g.216645047G=	NCBI36
NG_027721.1:g.64749G=
NG_027721.2:g.64749G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.347-87G= MANE Select	ENSP00000355897.4:n.347-87G=
ENST00000366929.4:c.431-87G=	ENSP00000355896.4:n.431-87G=
ENST00000366930.8:c.347-87G=	ENSP00000355897.4:n.347-87G=
ENST00000488793.1:n.11-87G=
NM_001135599.2:c.431-87G=	NP_001129071.1:n.431-87G=
NM_003238.3:c.347-87G=	NP_003229.1:n.347-87G=
NM_001135599.3:c.431-87G=	NP_001129071.1:n.431-87G=
NM_003238.4:c.347-87G=	NP_003229.1:n.347-87G=
NR_138148.1:n.1765-87G=
NR_138149.1:n.1849-87G=
NM_003238.5:c.347-87G=	NP_003229.1:n.347-87G=
NM_003238.6:c.347-87G= MANE Select	NP_003229.1:n.347-87G=
NM_001135599.4:c.431-87G=	NP_001129071.1:n.431-87G=
NR_138148.2:n.1713-87G=
NR_138149.2:n.1797-87G=