Canonical Allele Identifier: CA1221555835

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405213C= , CM000663.2:g.218405213C=	GRCh38
NC_000001.10:g.218578555C= , CM000663.1:g.218578555C=	GRCh37
NC_000001.9:g.216645178C=	NCBI36
NG_027721.1:g.64880C=
NG_027721.2:g.64880C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.391C= MANE Select	ENSP00000355897.4:p.Arg131=
ENST00000366929.4:c.475C=	ENSP00000355896.4:p.Arg159=
ENST00000366930.8:c.391C=	ENSP00000355897.4:p.Arg131=
ENST00000488793.1:n.55C=
NM_001135599.2:c.475C=	NP_001129071.1:p.Arg159=
NM_003238.3:c.391C=	NP_003229.1:p.Arg131=
NM_001135599.3:c.475C=	NP_001129071.1:p.Arg159=
NM_003238.4:c.391C=	NP_003229.1:p.Arg131=
NR_138148.1:n.1809C=
NR_138149.1:n.1893C=
NM_003238.5:c.391C=	NP_003229.1:p.Arg131=
NM_003238.6:c.391C= MANE Select	NP_003229.1:p.Arg131=
NM_001135599.4:c.475C=	NP_001129071.1:p.Arg159=
NR_138148.2:n.1757C=
NR_138149.2:n.1841C=