Canonical Allele Identifier: CA2747782700

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218437536A>C , CM000663.2:g.218437536A>C	GRCh38
NC_000001.10:g.218610878A>C , CM000663.1:g.218610878A>C	GRCh37
NC_000001.9:g.216677501A>C	NCBI36
NG_027721.1:g.97203A>C
NG_027721.2:g.97203A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1086+40A>C MANE Select	ENSP00000355897.4:n.1086+40A>C
ENST00000366929.4:c.1170+40A>C	ENSP00000355896.4:n.1170+40A>C
ENST00000366930.8:c.1086+40A>C	ENSP00000355897.4:n.1086+40A>C
ENST00000479322.1:n.570+40A>C
NM_001135599.2:c.1170+40A>C	NP_001129071.1:n.1170+40A>C
NM_003238.3:c.1086+40A>C	NP_003229.1:n.1086+40A>C
NM_001135599.3:c.1170+40A>C	NP_001129071.1:n.1170+40A>C
NM_003238.4:c.1086+40A>C	NP_003229.1:n.1086+40A>C
NR_138148.1:n.2389+40A>C
NR_138149.1:n.2473+40A>C
NM_003238.5:c.1086+40A>C	NP_003229.1:n.1086+40A>C
NM_003238.6:c.1086+40A>C MANE Select	NP_003229.1:n.1086+40A>C
NM_001135599.4:c.1170+40A>C	NP_001129071.1:n.1170+40A>C
NR_138148.2:n.2337+40A>C
NR_138149.2:n.2421+40A>C