Canonical Allele Identifier: CA1221568523

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441583A= , CM000663.2:g.218441583A=	GRCh38
NC_000001.10:g.218614925A= , CM000663.1:g.218614925A=	GRCh37
NC_000001.9:g.216681548A=	NCBI36
NG_027721.1:g.101250A=
NG_027721.2:g.101250A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*221A= MANE Select	ENSP00000355897.4:n.*221A=
ENST00000366929.4:c.*221A=	ENSP00000355896.4:n.*221A=
ENST00000366930.8:c.*221A=	ENSP00000355897.4:n.*221A=
ENST00000479322.1:n.950A=
NM_001135599.2:c.*221A=	NP_001129071.1:n.*221A=
NM_003238.3:c.*221A=	NP_003229.1:n.*221A=
NM_001135599.3:c.*221A=	NP_001129071.1:n.*221A=
NM_003238.4:c.*221A=	NP_003229.1:n.*221A=
NR_138148.1:n.2769A=
NR_138149.1:n.2853A=
NM_003238.5:c.*221A=	NP_003229.1:n.*221A=
NM_003238.6:c.*221A= MANE Select	NP_003229.1:n.*221A=
NM_001135599.4:c.*221A=	NP_001129071.1:n.*221A=
NR_138148.2:n.2717A=
NR_138149.2:n.2801A=