Canonical Allele Identifier: CA1221528755

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218347066T= , CM000663.2:g.218347066T=	GRCh38
NC_000001.10:g.218520408T= , CM000663.1:g.218520408T=	GRCh37
NC_000001.9:g.216587031T=	NCBI36
NG_027721.1:g.6733T=
NG_027721.2:g.6733T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.346+19T= MANE Select	ENSP00000355897.4:n.346+19T=
ENST00000366929.4:c.346+19T=	ENSP00000355896.4:n.346+19T=
ENST00000366930.8:c.346+19T=	ENSP00000355897.4:n.346+19T=
ENST00000488793.1:n.10+19T=
NM_001135599.2:c.346+19T=	NP_001129071.1:n.346+19T=
NM_003238.3:c.346+19T=	NP_003229.1:n.346+19T=
NM_001135599.3:c.346+19T=	NP_001129071.1:n.346+19T=
NM_003238.4:c.346+19T=	NP_003229.1:n.346+19T=
NR_138148.1:n.1764+19T=
NR_138149.1:n.1764+19T=
NM_003238.5:c.346+19T=	NP_003229.1:n.346+19T=
NM_003238.6:c.346+19T= MANE Select	NP_003229.1:n.346+19T=
NM_001135599.4:c.346+19T=	NP_001129071.1:n.346+19T=
NR_138148.2:n.1712+19T=
NR_138149.2:n.1712+19T=