Canonical Allele Identifier: CA3071756590

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405192A= , CM000663.2:g.218405192A=	GRCh38
NC_000001.10:g.218578534A= , CM000663.1:g.218578534A=	GRCh37
NC_000001.9:g.216645157A=	NCBI36
NG_027721.1:g.64859A=
NG_027721.2:g.64859A=

Transcript Alleles

HGVS	Amino-acid Change
NM_003238.6:c.370A= MANE Select	NP_003229.1:p.Arg124=
ENST00000366930.9:c.370A= MANE Select	ENSP00000355897.4:p.Arg124=
NM_001135599.2:c.454A=	NP_001129071.1:p.Arg152=
NM_001135599.3:c.454A=	NP_001129071.1:p.Arg152=
NM_001135599.4:c.454A=	NP_001129071.1:p.Arg152=
NM_003238.3:c.370A=	NP_003229.1:p.Arg124=
NM_003238.4:c.370A=	NP_003229.1:p.Arg124=
NM_003238.5:c.370A=	NP_003229.1:p.Arg124=
NR_138148.1:n.1788A=
NR_138148.2:n.1736A=
NR_138149.1:n.1872A=
NR_138149.2:n.1820A=
ENST00000366929.4:c.454A=	ENSP00000355896.4:p.Arg152=
ENST00000366930.8:c.370A=	ENSP00000355897.4:p.Arg124=
ENST00000488793.1:n.34A=