Canonical Allele Identifier: CA1142193856

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437394G= , CM000663.2:g.218437394G=	GRCh38
NC_000001.10:g.218610736G= , CM000663.1:g.218610736G=	GRCh37
NC_000001.9:g.216677359G=	NCBI36
NG_027721.1:g.97061G=
NG_027721.2:g.97061G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.984G= MANE Select	ENSP00000355897.4:p.Arg328=
ENST00000366929.4:c.1068G=	ENSP00000355896.4:p.Arg356=
ENST00000366930.8:c.984G=	ENSP00000355897.4:p.Arg328=
ENST00000479322.1:n.468G=
NM_001135599.2:c.1068G=	NP_001129071.1:p.Arg356=
NM_003238.3:c.984G=	NP_003229.1:p.Arg328=
NM_001135599.3:c.1068G=	NP_001129071.1:p.Arg356=
NM_003238.4:c.984G=	NP_003229.1:p.Arg328=
NR_138148.1:n.2287G=
NR_138149.1:n.2371G=
NM_003238.5:c.984G=	NP_003229.1:p.Arg328=
NM_003238.6:c.984G= MANE Select	NP_003229.1:p.Arg328=
NM_001135599.4:c.1068G=	NP_001129071.1:p.Arg356=
NR_138148.2:n.2235G=
NR_138149.2:n.2319G=