Canonical Allele Identifier: CA1221566042

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437348T= , CM000663.2:g.218437348T=	GRCh38
NC_000001.10:g.218610690T= , CM000663.1:g.218610690T=	GRCh37
NC_000001.9:g.216677313T=	NCBI36
NG_027721.1:g.97015T=
NG_027721.2:g.97015T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.938T= MANE Select	ENSP00000355897.4:p.Val313=
ENST00000366929.4:c.1022T=	ENSP00000355896.4:p.Val341=
ENST00000366930.8:c.938T=	ENSP00000355897.4:p.Val313=
ENST00000479322.1:n.422T=
NM_001135599.2:c.1022T=	NP_001129071.1:p.Val341=
NM_003238.3:c.938T=	NP_003229.1:p.Val313=
NM_001135599.3:c.1022T=	NP_001129071.1:p.Val341=
NM_003238.4:c.938T=	NP_003229.1:p.Val313=
NR_138148.1:n.2241T=
NR_138149.1:n.2325T=
NM_003238.5:c.938T=	NP_003229.1:p.Val313=
NM_003238.6:c.938T= MANE Select	NP_003229.1:p.Val313=
NM_001135599.4:c.1022T=	NP_001129071.1:p.Val341=
NR_138148.2:n.2189T=
NR_138149.2:n.2273T=