Canonical Allele Identifier: CA2650531402

Gene: TGFB2

Linked Data

• gnomAD v4: 1-218434271-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218434271A>C , CM000663.2:g.218434271A>C	GRCh38
NC_000001.10:g.218607613A>C , CM000663.1:g.218607613A>C	GRCh37
NC_000001.9:g.216674236A>C	NCBI36
NG_027721.1:g.93938A>C
NG_027721.2:g.93938A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.643+57A>C MANE Select	ENSP00000355897.4:n.643+57A>C
ENST00000366929.4:c.727+57A>C	ENSP00000355896.4:n.727+57A>C
ENST00000366930.8:c.643+57A>C	ENSP00000355897.4:n.643+57A>C
ENST00000479322.1:n.127+19A>C
ENST00000488793.1:n.364A>C
NM_001135599.2:c.727+57A>C	NP_001129071.1:n.727+57A>C
NM_003238.3:c.643+57A>C	NP_003229.1:n.643+57A>C
NM_001135599.3:c.727+57A>C	NP_001129071.1:n.727+57A>C
NM_003238.4:c.643+57A>C	NP_003229.1:n.643+57A>C
NR_138148.1:n.2061+57A>C
NR_138149.1:n.2145+57A>C
NM_003238.5:c.643+57A>C	NP_003229.1:n.643+57A>C
NM_003238.6:c.643+57A>C MANE Select	NP_003229.1:n.643+57A>C
NM_001135599.4:c.727+57A>C	NP_001129071.1:n.727+57A>C
NR_138148.2:n.2009+57A>C
NR_138149.2:n.2093+57A>C