Canonical Allele Identifier: CA1221564959

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218436111G= , CM000663.2:g.218436111G=	GRCh38
NC_000001.10:g.218609453G= , CM000663.1:g.218609453G=	GRCh37
NC_000001.9:g.216676076G=	NCBI36
NG_027721.1:g.95778G=
NG_027721.2:g.95778G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.896G= MANE Select	ENSP00000355897.4:p.Arg299=
ENST00000366929.4:c.980G=	ENSP00000355896.4:p.Arg327=
ENST00000366930.8:c.896G=	ENSP00000355897.4:p.Arg299=
ENST00000479322.1:n.380G=
NM_001135599.2:c.980G=	NP_001129071.1:p.Arg327=
NM_003238.3:c.896G=	NP_003229.1:p.Arg299=
NM_001135599.3:c.980G=	NP_001129071.1:p.Arg327=
NM_003238.4:c.896G=	NP_003229.1:p.Arg299=
NR_138148.1:n.2199G=
NR_138149.1:n.2283G=
NM_003238.5:c.896G=	NP_003229.1:p.Arg299=
NM_003238.6:c.896G= MANE Select	NP_003229.1:p.Arg299=
NM_001135599.4:c.980G=	NP_001129071.1:p.Arg327=
NR_138148.2:n.2147G=
NR_138149.2:n.2231G=