Canonical Allele Identifier: CA1221564972

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218436119C= , CM000663.2:g.218436119C=	GRCh38
NC_000001.10:g.218609461C= , CM000663.1:g.218609461C=	GRCh37
NC_000001.9:g.216676084C=	NCBI36
NG_027721.1:g.95786C=
NG_027721.2:g.95786C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.904C= MANE Select	ENSP00000355897.4:p.Arg302=
ENST00000366929.4:c.988C=	ENSP00000355896.4:p.Arg330=
ENST00000366930.8:c.904C=	ENSP00000355897.4:p.Arg302=
ENST00000479322.1:n.388C=
NM_001135599.2:c.988C=	NP_001129071.1:p.Arg330=
NM_003238.3:c.904C=	NP_003229.1:p.Arg302=
NM_001135599.3:c.988C=	NP_001129071.1:p.Arg330=
NM_003238.4:c.904C=	NP_003229.1:p.Arg302=
NR_138148.1:n.2207C=
NR_138149.1:n.2291C=
NM_003238.5:c.904C=	NP_003229.1:p.Arg302=
NM_003238.6:c.904C= MANE Select	NP_003229.1:p.Arg302=
NM_001135599.4:c.988C=	NP_001129071.1:p.Arg330=
NR_138148.2:n.2155C=
NR_138149.2:n.2239C=