Canonical Allele Identifier: CA1141097755

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437336T= , CM000663.2:g.218437336T=	GRCh38
NC_000001.10:g.218610678T= , CM000663.1:g.218610678T=	GRCh37
NC_000001.9:g.216677301T=	NCBI36
NG_027721.1:g.97003T=
NG_027721.2:g.97003T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.933-7T= MANE Select	ENSP00000355897.4:n.933-7T=
ENST00000366929.4:c.1017-7T=	ENSP00000355896.4:n.1017-7T=
ENST00000366930.8:c.933-7T=	ENSP00000355897.4:n.933-7T=
ENST00000479322.1:n.417-7T=
NM_001135599.2:c.1017-7T=	NP_001129071.1:n.1017-7T=
NM_003238.3:c.933-7T=	NP_003229.1:n.933-7T=
NM_001135599.3:c.1017-7T=	NP_001129071.1:n.1017-7T=
NM_003238.4:c.933-7T=	NP_003229.1:n.933-7T=
NR_138148.1:n.2236-7T=
NR_138149.1:n.2320-7T=
NM_003238.5:c.933-7T=	NP_003229.1:n.933-7T=
NM_003238.6:c.933-7T= MANE Select	NP_003229.1:n.933-7T=
NM_001135599.4:c.1017-7T=	NP_001129071.1:n.1017-7T=
NR_138148.2:n.2184-7T=
NR_138149.2:n.2268-7T=