Canonical Allele Identifier: CA1221528588

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346660T= , CM000663.2:g.218346660T=	GRCh38
NC_000001.10:g.218520002T= , CM000663.1:g.218520002T=	GRCh37
NC_000001.9:g.216586625T=	NCBI36
NG_027721.1:g.6327T=
NG_027721.2:g.6327T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-42T= MANE Select	ENSP00000355897.4:n.-42T=
ENST00000366929.4:c.-42T=	ENSP00000355896.4:n.-42T=
ENST00000366930.8:c.-42T=	ENSP00000355897.4:n.-42T=
NM_001135599.2:c.-42T=	NP_001129071.1:n.-42T=
NM_003238.3:c.-42T=	NP_003229.1:n.-42T=
NM_001135599.3:c.-42T=	NP_001129071.1:n.-42T=
NM_003238.4:c.-42T=	NP_003229.1:n.-42T=
NR_138148.1:n.1377T=
NR_138149.1:n.1377T=
NM_003238.5:c.-42T=	NP_003229.1:n.-42T=
NM_003238.6:c.-42T= MANE Select	NP_003229.1:n.-42T=
NM_001135599.4:c.-42T=	NP_001129071.1:n.-42T=
NR_138148.2:n.1325T=
NR_138149.2:n.1325T=