Canonical Allele Identifier: CA1221563018

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218434074C= , CM000663.2:g.218434074C=	GRCh38
NC_000001.10:g.218607416C= , CM000663.1:g.218607416C=	GRCh37
NC_000001.9:g.216674039C=	NCBI36
NG_027721.1:g.93741C=
NG_027721.2:g.93741C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.511-8C= MANE Select	ENSP00000355897.4:n.511-8C=
ENST00000366929.4:c.595-8C=	ENSP00000355896.4:n.595-8C=
ENST00000366930.8:c.511-8C=	ENSP00000355897.4:n.511-8C=
ENST00000488793.1:n.175-8C=
NM_001135599.2:c.595-8C=	NP_001129071.1:n.595-8C=
NM_003238.3:c.511-8C=	NP_003229.1:n.511-8C=
NM_001135599.3:c.595-8C=	NP_001129071.1:n.595-8C=
NM_003238.4:c.511-8C=	NP_003229.1:n.511-8C=
NR_138148.1:n.1929-8C=
NR_138149.1:n.2013-8C=
NM_003238.5:c.511-8C=	NP_003229.1:n.511-8C=
NM_003238.6:c.511-8C= MANE Select	NP_003229.1:n.511-8C=
NM_001135599.4:c.595-8C=	NP_001129071.1:n.595-8C=
NR_138148.2:n.1877-8C=
NR_138149.2:n.1961-8C=