Canonical Allele Identifier: CA1221568466

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441442C= , CM000663.2:g.218441442C=	GRCh38
NC_000001.10:g.218614784C= , CM000663.1:g.218614784C=	GRCh37
NC_000001.9:g.216681407C=	NCBI36
NG_027721.1:g.101109C=
NG_027721.2:g.101109C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*80C= MANE Select	ENSP00000355897.4:n.*80C=
ENST00000366929.4:c.*80C=	ENSP00000355896.4:n.*80C=
ENST00000366930.8:c.*80C=	ENSP00000355897.4:n.*80C=
ENST00000479322.1:n.809C=
NM_001135599.2:c.*80C=	NP_001129071.1:n.*80C=
NM_003238.3:c.*80C=	NP_003229.1:n.*80C=
NM_001135599.3:c.*80C=	NP_001129071.1:n.*80C=
NM_003238.4:c.*80C=	NP_003229.1:n.*80C=
NR_138148.1:n.2628C=
NR_138149.1:n.2712C=
NM_003238.5:c.*80C=	NP_003229.1:n.*80C=
NM_003238.6:c.*80C= MANE Select	NP_003229.1:n.*80C=
NM_001135599.4:c.*80C=	NP_001129071.1:n.*80C=
NR_138148.2:n.2576C=
NR_138149.2:n.2660C=