Canonical Allele Identifier: CA1221568441

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441411A= , CM000663.2:g.218441411A=	GRCh38
NC_000001.10:g.218614753A= , CM000663.1:g.218614753A=	GRCh37
NC_000001.9:g.216681376A=	NCBI36
NG_027721.1:g.101078A=
NG_027721.2:g.101078A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*49A= MANE Select	ENSP00000355897.4:n.*49A=
ENST00000366929.4:c.*49A=	ENSP00000355896.4:n.*49A=
ENST00000366930.8:c.*49A=	ENSP00000355897.4:n.*49A=
ENST00000479322.1:n.778A=
NM_001135599.2:c.*49A=	NP_001129071.1:n.*49A=
NM_003238.3:c.*49A=	NP_003229.1:n.*49A=
NM_001135599.3:c.*49A=	NP_001129071.1:n.*49A=
NM_003238.4:c.*49A=	NP_003229.1:n.*49A=
NR_138148.1:n.2597A=
NR_138149.1:n.2681A=
NM_003238.5:c.*49A=	NP_003229.1:n.*49A=
NM_003238.6:c.*49A= MANE Select	NP_003229.1:n.*49A=
NM_001135599.4:c.*49A=	NP_001129071.1:n.*49A=
NR_138148.2:n.2545A=
NR_138149.2:n.2629A=