Canonical Allele Identifier: CA1398461

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405323G>A , CM000663.2:g.218405323G>A	GRCh38
NC_000001.10:g.218578665G>A , CM000663.1:g.218578665G>A	GRCh37
NC_000001.9:g.216645288G>A	NCBI36
NG_027721.1:g.64990G>A
NG_027721.2:g.64990G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003238.6:c.501G>A MANE Select	NP_003229.1:p.Glu167=
ENST00000366930.9:c.501G>A MANE Select	ENSP00000355897.4:p.Glu167=
NM_001135599.2:c.585G>A	NP_001129071.1:p.Glu195=
NM_001135599.3:c.585G>A	NP_001129071.1:p.Glu195=
NM_001135599.4:c.585G>A	NP_001129071.1:p.Glu195=
NM_003238.3:c.501G>A	NP_003229.1:p.Glu167=
NM_003238.4:c.501G>A	NP_003229.1:p.Glu167=
NM_003238.5:c.501G>A	NP_003229.1:p.Glu167=
NR_138148.1:n.1919G>A
NR_138148.2:n.1867G>A
NR_138149.1:n.2003G>A
NR_138149.2:n.1951G>A
ENST00000366929.4:c.585G>A	ENSP00000355896.4:p.Glu195=
ENST00000366930.8:c.501G>A	ENSP00000355897.4:p.Glu167=
ENST00000488793.1:n.165G>A