Canonical Allele Identifier: CA1146380014

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346711T= , CM000663.2:g.218346711T=	GRCh38
NC_000001.10:g.218520053T= , CM000663.1:g.218520053T=	GRCh37
NC_000001.9:g.216586676T=	NCBI36
NG_027721.1:g.6378T=
NG_027721.2:g.6378T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.10T= MANE Select	ENSP00000355897.4:p.Cys4=
ENST00000366929.4:c.10T=	ENSP00000355896.4:p.Cys4=
ENST00000366930.8:c.10T=	ENSP00000355897.4:p.Cys4=
NM_001135599.2:c.10T=	NP_001129071.1:p.Cys4=
NM_003238.3:c.10T=	NP_003229.1:p.Cys4=
NM_001135599.3:c.10T=	NP_001129071.1:p.Cys4=
NM_003238.4:c.10T=	NP_003229.1:p.Cys4=
NR_138148.1:n.1428T=
NR_138149.1:n.1428T=
NM_003238.5:c.10T=	NP_003229.1:p.Cys4=
NM_003238.6:c.10T= MANE Select	NP_003229.1:p.Cys4=
NM_001135599.4:c.10T=	NP_001129071.1:p.Cys4=
NR_138148.2:n.1376T=
NR_138149.2:n.1376T=