Canonical Allele Identifier: CA1221565901

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437272A= , CM000663.2:g.218437272A=	GRCh38
NC_000001.10:g.218610614A= , CM000663.1:g.218610614A=	GRCh37
NC_000001.9:g.216677237A=	NCBI36
NG_027721.1:g.96939A=
NG_027721.2:g.96939A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.933-71A= MANE Select	ENSP00000355897.4:n.933-71A=
ENST00000366929.4:c.1017-71A=	ENSP00000355896.4:n.1017-71A=
ENST00000366930.8:c.933-71A=	ENSP00000355897.4:n.933-71A=
ENST00000479322.1:n.417-71A=
NM_001135599.2:c.1017-71A=	NP_001129071.1:n.1017-71A=
NM_003238.3:c.933-71A=	NP_003229.1:n.933-71A=
NM_001135599.3:c.1017-71A=	NP_001129071.1:n.1017-71A=
NM_003238.4:c.933-71A=	NP_003229.1:n.933-71A=
NR_138148.1:n.2236-71A=
NR_138149.1:n.2320-71A=
NM_003238.5:c.933-71A=	NP_003229.1:n.933-71A=
NM_003238.6:c.933-71A= MANE Select	NP_003229.1:n.933-71A=
NM_001135599.4:c.1017-71A=	NP_001129071.1:n.1017-71A=
NR_138148.2:n.2184-71A=
NR_138149.2:n.2268-71A=