Canonical Allele Identifier: CA1221555728

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405102C= , CM000663.2:g.218405102C=	GRCh38
NC_000001.10:g.218578444C= , CM000663.1:g.218578444C=	GRCh37
NC_000001.9:g.216645067C=	NCBI36
NG_027721.1:g.64769C=
NG_027721.2:g.64769C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.347-67C= MANE Select	ENSP00000355897.4:n.347-67C=
ENST00000366929.4:c.431-67C=	ENSP00000355896.4:n.431-67C=
ENST00000366930.8:c.347-67C=	ENSP00000355897.4:n.347-67C=
ENST00000488793.1:n.11-67C=
NM_001135599.2:c.431-67C=	NP_001129071.1:n.431-67C=
NM_003238.3:c.347-67C=	NP_003229.1:n.347-67C=
NM_001135599.3:c.431-67C=	NP_001129071.1:n.431-67C=
NM_003238.4:c.347-67C=	NP_003229.1:n.347-67C=
NR_138148.1:n.1765-67C=
NR_138149.1:n.1849-67C=
NM_003238.5:c.347-67C=	NP_003229.1:n.347-67C=
NM_003238.6:c.347-67C= MANE Select	NP_003229.1:n.347-67C=
NM_001135599.4:c.431-67C=	NP_001129071.1:n.431-67C=
NR_138148.2:n.1713-67C=
NR_138149.2:n.1797-67C=