Canonical Allele Identifier: CA1149038289

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437443T= , CM000663.2:g.218437443T=	GRCh38
NC_000001.10:g.218610785T= , CM000663.1:g.218610785T=	GRCh37
NC_000001.9:g.216677408T=	NCBI36
NG_027721.1:g.97110T=
NG_027721.2:g.97110T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1033T= MANE Select	ENSP00000355897.4:p.Phe345=
ENST00000366929.4:c.1117T=	ENSP00000355896.4:p.Phe373=
ENST00000366930.8:c.1033T=	ENSP00000355897.4:p.Phe345=
ENST00000479322.1:n.517T=
NM_001135599.2:c.1117T=	NP_001129071.1:p.Phe373=
NM_003238.3:c.1033T=	NP_003229.1:p.Phe345=
NM_001135599.3:c.1117T=	NP_001129071.1:p.Phe373=
NM_003238.4:c.1033T=	NP_003229.1:p.Phe345=
NR_138148.1:n.2336T=
NR_138149.1:n.2420T=
NM_003238.5:c.1033T=	NP_003229.1:p.Phe345=
NM_003238.6:c.1033T= MANE Select	NP_003229.1:p.Phe345=
NM_001135599.4:c.1117T=	NP_001129071.1:p.Phe373=
NR_138148.2:n.2284T=
NR_138149.2:n.2368T=