Canonical Allele Identifier: CA1221568336

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441162C= , CM000663.2:g.218441162C=	GRCh38
NC_000001.10:g.218614504C= , CM000663.1:g.218614504C=	GRCh37
NC_000001.9:g.216681127C=	NCBI36
NG_027721.1:g.100829C=
NG_027721.2:g.100829C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1087-42C= MANE Select	ENSP00000355897.4:n.1087-42C=
ENST00000366929.4:c.1171-42C=	ENSP00000355896.4:n.1171-42C=
ENST00000366930.8:c.1087-42C=	ENSP00000355897.4:n.1087-42C=
ENST00000479322.1:n.571-42C=
NM_001135599.2:c.1171-42C=	NP_001129071.1:n.1171-42C=
NM_003238.3:c.1087-42C=	NP_003229.1:n.1087-42C=
NM_001135599.3:c.1171-42C=	NP_001129071.1:n.1171-42C=
NM_003238.4:c.1087-42C=	NP_003229.1:n.1087-42C=
NR_138148.1:n.2390-42C=
NR_138149.1:n.2474-42C=
NM_003238.5:c.1087-42C=	NP_003229.1:n.1087-42C=
NM_003238.6:c.1087-42C= MANE Select	NP_003229.1:n.1087-42C=
NM_001135599.4:c.1171-42C=	NP_001129071.1:n.1171-42C=
NR_138148.2:n.2338-42C=
NR_138149.2:n.2422-42C=