Canonical Allele Identifier: CA1148225009

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218434115C= , CM000663.2:g.218434115C=	GRCh38
NC_000001.10:g.218607457C= , CM000663.1:g.218607457C=	GRCh37
NC_000001.9:g.216674080C=	NCBI36
NG_027721.1:g.93782C=
NG_027721.2:g.93782C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.544C= MANE Select	ENSP00000355897.4:p.Gln182=
ENST00000366929.4:c.628C=	ENSP00000355896.4:p.Gln210=
ENST00000366930.8:c.544C=	ENSP00000355897.4:p.Gln182=
ENST00000488793.1:n.208C=
NM_001135599.2:c.628C=	NP_001129071.1:p.Gln210=
NM_003238.3:c.544C=	NP_003229.1:p.Gln182=
NM_001135599.3:c.628C=	NP_001129071.1:p.Gln210=
NM_003238.4:c.544C=	NP_003229.1:p.Gln182=
NR_138148.1:n.1962C=
NR_138149.1:n.2046C=
NM_003238.5:c.544C=	NP_003229.1:p.Gln182=
NM_003238.6:c.544C= MANE Select	NP_003229.1:p.Gln182=
NM_001135599.4:c.628C=	NP_001129071.1:p.Gln210=
NR_138148.2:n.1910C=
NR_138149.2:n.1994C=