Canonical Allele Identifier: CA1143974046

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218434258C= , CM000663.2:g.218434258C=	GRCh38
NC_000001.10:g.218607600C= , CM000663.1:g.218607600C=	GRCh37
NC_000001.9:g.216674223C=	NCBI36
NG_027721.1:g.93925C=
NG_027721.2:g.93925C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.643+44C= MANE Select	ENSP00000355897.4:n.643+44C=
ENST00000366929.4:c.727+44C=	ENSP00000355896.4:n.727+44C=
ENST00000366930.8:c.643+44C=	ENSP00000355897.4:n.643+44C=
ENST00000479322.1:n.127+6C=
ENST00000488793.1:n.351C=
NM_001135599.2:c.727+44C=	NP_001129071.1:n.727+44C=
NM_003238.3:c.643+44C=	NP_003229.1:n.643+44C=
NM_001135599.3:c.727+44C=	NP_001129071.1:n.727+44C=
NM_003238.4:c.643+44C=	NP_003229.1:n.643+44C=
NR_138148.1:n.2061+44C=
NR_138149.1:n.2145+44C=
NM_003238.5:c.643+44C=	NP_003229.1:n.643+44C=
NM_003238.6:c.643+44C= MANE Select	NP_003229.1:n.643+44C=
NM_001135599.4:c.727+44C=	NP_001129071.1:n.727+44C=
NR_138148.2:n.2009+44C=
NR_138149.2:n.2093+44C=