Canonical Allele Identifier: CA1221563357

Gene: TGFB2

Linked Data

• dbSNP Id: rs1659900239
• gnomAD v4: 1-218434245-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218434245G>A , CM000663.2:g.218434245G>A	GRCh38
NC_000001.10:g.218607587G>A , CM000663.1:g.218607587G>A	GRCh37
NC_000001.9:g.216674210G>A	NCBI36
NG_027721.1:g.93912G>A
NG_027721.2:g.93912G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.643+31G>A MANE Select	ENSP00000355897.4:n.643+31G>A
ENST00000366929.4:c.727+31G>A	ENSP00000355896.4:n.727+31G>A
ENST00000366930.8:c.643+31G>A	ENSP00000355897.4:n.643+31G>A
ENST00000479322.1:n.120G>A
ENST00000488793.1:n.338G>A
NM_001135599.2:c.727+31G>A	NP_001129071.1:n.727+31G>A
NM_003238.3:c.643+31G>A	NP_003229.1:n.643+31G>A
NM_001135599.3:c.727+31G>A	NP_001129071.1:n.727+31G>A
NM_003238.4:c.643+31G>A	NP_003229.1:n.643+31G>A
NR_138148.1:n.2061+31G>A
NR_138149.1:n.2145+31G>A
NM_003238.5:c.643+31G>A	NP_003229.1:n.643+31G>A
NM_003238.6:c.643+31G>A MANE Select	NP_003229.1:n.643+31G>A
NM_001135599.4:c.727+31G>A	NP_001129071.1:n.727+31G>A
NR_138148.2:n.2009+31G>A
NR_138149.2:n.2093+31G>A