Canonical Allele Identifier: CA1144229221

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437423C= , CM000663.2:g.218437423C=	GRCh38
NC_000001.10:g.218610765C= , CM000663.1:g.218610765C=	GRCh37
NC_000001.9:g.216677388C=	NCBI36
NG_027721.1:g.97090C=
NG_027721.2:g.97090C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.1013C= MANE Select	ENSP00000355897.4:p.Pro338=
ENST00000366929.4:c.1097C=	ENSP00000355896.4:p.Pro366=
ENST00000366930.8:c.1013C=	ENSP00000355897.4:p.Pro338=
ENST00000479322.1:n.497C=
NM_001135599.2:c.1097C=	NP_001129071.1:p.Pro366=
NM_003238.3:c.1013C=	NP_003229.1:p.Pro338=
NM_001135599.3:c.1097C=	NP_001129071.1:p.Pro366=
NM_003238.4:c.1013C=	NP_003229.1:p.Pro338=
NR_138148.1:n.2316C=
NR_138149.1:n.2400C=
NM_003238.5:c.1013C=	NP_003229.1:p.Pro338=
NM_003238.6:c.1013C= MANE Select	NP_003229.1:p.Pro338=
NM_001135599.4:c.1097C=	NP_001129071.1:p.Pro366=
NR_138148.2:n.2264C=
NR_138149.2:n.2348C=