Canonical Allele Identifier: CA1221568464

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441441A= , CM000663.2:g.218441441A=	GRCh38
NC_000001.10:g.218614783A= , CM000663.1:g.218614783A=	GRCh37
NC_000001.9:g.216681406A=	NCBI36
NG_027721.1:g.101108A=
NG_027721.2:g.101108A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*79A= MANE Select	ENSP00000355897.4:n.*79A=
ENST00000366929.4:c.*79A=	ENSP00000355896.4:n.*79A=
ENST00000366930.8:c.*79A=	ENSP00000355897.4:n.*79A=
ENST00000479322.1:n.808A=
NM_001135599.2:c.*79A=	NP_001129071.1:n.*79A=
NM_003238.3:c.*79A=	NP_003229.1:n.*79A=
NM_001135599.3:c.*79A=	NP_001129071.1:n.*79A=
NM_003238.4:c.*79A=	NP_003229.1:n.*79A=
NR_138148.1:n.2627A=
NR_138149.1:n.2711A=
NM_003238.5:c.*79A=	NP_003229.1:n.*79A=
NM_003238.6:c.*79A= MANE Select	NP_003229.1:n.*79A=
NM_001135599.4:c.*79A=	NP_001129071.1:n.*79A=
NR_138148.2:n.2575A=
NR_138149.2:n.2659A=