Canonical Allele Identifier: CA1221528696

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346914C= , CM000663.2:g.218346914C=	GRCh38
NC_000001.10:g.218520256C= , CM000663.1:g.218520256C=	GRCh37
NC_000001.9:g.216586879C=	NCBI36
NG_027721.1:g.6581C=
NG_027721.2:g.6581C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.213C= MANE Select	ENSP00000355897.4:p.Tyr71=
ENST00000366929.4:c.213C=	ENSP00000355896.4:p.Tyr71=
ENST00000366930.8:c.213C=	ENSP00000355897.4:p.Tyr71=
NM_001135599.2:c.213C=	NP_001129071.1:p.Tyr71=
NM_003238.3:c.213C=	NP_003229.1:p.Tyr71=
NM_001135599.3:c.213C=	NP_001129071.1:p.Tyr71=
NM_003238.4:c.213C=	NP_003229.1:p.Tyr71=
NR_138148.1:n.1631C=
NR_138149.1:n.1631C=
NM_003238.5:c.213C=	NP_003229.1:p.Tyr71=
NM_003238.6:c.213C= MANE Select	NP_003229.1:p.Tyr71=
NM_001135599.4:c.213C=	NP_001129071.1:p.Tyr71=
NR_138148.2:n.1579C=
NR_138149.2:n.1579C=