Canonical Allele Identifier: CA1221555809

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405184C= , CM000663.2:g.218405184C=	GRCh38
NC_000001.10:g.218578526C= , CM000663.1:g.218578526C=	GRCh37
NC_000001.9:g.216645149C=	NCBI36
NG_027721.1:g.64851C=
NG_027721.2:g.64851C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.362C= MANE Select	ENSP00000355897.4:p.Thr121=
ENST00000366929.4:c.446C=	ENSP00000355896.4:p.Thr149=
ENST00000366930.8:c.362C=	ENSP00000355897.4:p.Thr121=
ENST00000488793.1:n.26C=
NM_001135599.2:c.446C=	NP_001129071.1:p.Thr149=
NM_003238.3:c.362C=	NP_003229.1:p.Thr121=
NM_001135599.3:c.446C=	NP_001129071.1:p.Thr149=
NM_003238.4:c.362C=	NP_003229.1:p.Thr121=
NR_138148.1:n.1780C=
NR_138149.1:n.1864C=
NM_003238.5:c.362C=	NP_003229.1:p.Thr121=
NM_003238.6:c.362C= MANE Select	NP_003229.1:p.Thr121=
NM_001135599.4:c.446C=	NP_001129071.1:p.Thr149=
NR_138148.2:n.1728C=
NR_138149.2:n.1812C=