Canonical Allele Identifier: CA1221565019

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218436147G= , CM000663.2:g.218436147G=	GRCh38
NC_000001.10:g.218609489G= , CM000663.1:g.218609489G=	GRCh37
NC_000001.9:g.216676112G=	NCBI36
NG_027721.1:g.95814G=
NG_027721.2:g.95814G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003238.6:c.932G= MANE Select	NP_003229.1:p.Arg311=
ENST00000366930.9:c.932G= MANE Select	ENSP00000355897.4:p.Arg311=
NM_001135599.2:c.1016G=	NP_001129071.1:p.Arg339=
NM_001135599.3:c.1016G=	NP_001129071.1:p.Arg339=
NM_001135599.4:c.1016G=	NP_001129071.1:p.Arg339=
NM_003238.3:c.932G=	NP_003229.1:p.Arg311=
NM_003238.4:c.932G=	NP_003229.1:p.Arg311=
NM_003238.5:c.932G=	NP_003229.1:p.Arg311=
NR_138148.1:n.2235G=
NR_138148.2:n.2183G=
NR_138149.1:n.2319G=
NR_138149.2:n.2267G=
ENST00000366929.4:c.1016G=	ENSP00000355896.4:p.Arg339=
ENST00000366930.8:c.932G=	ENSP00000355897.4:p.Arg311=
ENST00000479322.1:n.416G=