Canonical Allele Identifier: CA1221528649

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346789G= , CM000663.2:g.218346789G=	GRCh38
NC_000001.10:g.218520131G= , CM000663.1:g.218520131G=	GRCh37
NC_000001.9:g.216586754G=	NCBI36
NG_027721.1:g.6456G=
NG_027721.2:g.6456G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.88G= MANE Select	ENSP00000355897.4:p.Asp30=
ENST00000366929.4:c.88G=	ENSP00000355896.4:p.Asp30=
ENST00000366930.8:c.88G=	ENSP00000355897.4:p.Asp30=
NM_001135599.2:c.88G=	NP_001129071.1:p.Asp30=
NM_003238.3:c.88G=	NP_003229.1:p.Asp30=
NM_001135599.3:c.88G=	NP_001129071.1:p.Asp30=
NM_003238.4:c.88G=	NP_003229.1:p.Asp30=
NR_138148.1:n.1506G=
NR_138149.1:n.1506G=
NM_003238.5:c.88G=	NP_003229.1:p.Asp30=
NM_003238.6:c.88G= MANE Select	NP_003229.1:p.Asp30=
NM_001135599.4:c.88G=	NP_001129071.1:p.Asp30=
NR_138148.2:n.1454G=
NR_138149.2:n.1454G=