Canonical Allele Identifier: CA1221566191

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437428G= , CM000663.2:g.218437428G=	GRCh38
NC_000001.10:g.218610770G= , CM000663.1:g.218610770G=	GRCh37
NC_000001.9:g.216677393G=	NCBI36
NG_027721.1:g.97095G=
NG_027721.2:g.97095G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.1018G= MANE Select	ENSP00000355897.4:p.Gly340=
ENST00000366929.4:c.1102G=	ENSP00000355896.4:p.Gly368=
ENST00000366930.8:c.1018G=	ENSP00000355897.4:p.Gly340=
ENST00000479322.1:n.502G=
NM_001135599.2:c.1102G=	NP_001129071.1:p.Gly368=
NM_003238.3:c.1018G=	NP_003229.1:p.Gly340=
NM_001135599.3:c.1102G=	NP_001129071.1:p.Gly368=
NM_003238.4:c.1018G=	NP_003229.1:p.Gly340=
NR_138148.1:n.2321G=
NR_138149.1:n.2405G=
NM_003238.5:c.1018G=	NP_003229.1:p.Gly340=
NM_003238.6:c.1018G= MANE Select	NP_003229.1:p.Gly340=
NM_001135599.4:c.1102G=	NP_001129071.1:p.Gly368=
NR_138148.2:n.2269G=
NR_138149.2:n.2353G=