Canonical Allele Identifier: CA1221568407

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441361A= , CM000663.2:g.218441361A=	GRCh38
NC_000001.10:g.218614703A= , CM000663.1:g.218614703A=	GRCh37
NC_000001.9:g.216681326A=	NCBI36
NG_027721.1:g.101028A=
NG_027721.2:g.101028A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1244A= MANE Select	ENSP00000355897.4:p.Ter415=
ENST00000366929.4:c.1328A=	ENSP00000355896.4:p.Ter443=
ENST00000366930.8:c.1244A=	ENSP00000355897.4:p.Ter415=
ENST00000479322.1:n.728A=
NM_001135599.2:c.1328A=	NP_001129071.1:p.Ter443=
NM_003238.3:c.1244A=	NP_003229.1:p.Ter415=
NM_001135599.3:c.1328A=	NP_001129071.1:p.Ter443=
NM_003238.4:c.1244A=	NP_003229.1:p.Ter415=
NR_138148.1:n.2547A=
NR_138149.1:n.2631A=
NM_003238.5:c.1244A=	NP_003229.1:p.Ter415=
NM_003238.6:c.1244A= MANE Select	NP_003229.1:p.Ter415=
NM_001135599.4:c.1328A=	NP_001129071.1:p.Ter443=
NR_138148.2:n.2495A=
NR_138149.2:n.2579A=