Canonical Allele Identifier: CA423416100

Gene: TGFB2

Linked Data

• COSMIC: COSM5025513 ; COSM5025514
• MyVariant Identifiers: chr1:g.218607682A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218434340A>C , CM000663.2:g.218434340A>C	GRCh38
NC_000001.10:g.218607682A>C , CM000663.1:g.218607682A>C	GRCh37
NC_000001.9:g.216674305A>C	NCBI36
NG_027721.1:g.94007A>C
NG_027721.2:g.94007A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.646A>C MANE Select	ENSP00000355897.4:p.Arg216=
ENST00000366929.4:c.730A>C	ENSP00000355896.4:p.Arg244=
ENST00000366930.8:c.646A>C	ENSP00000355897.4:p.Arg216=
ENST00000479322.1:n.130A>C
NM_001135599.2:c.730A>C	NP_001129071.1:p.Arg244=
NM_003238.3:c.646A>C	NP_003229.1:p.Arg216=
NM_001135599.3:c.730A>C	NP_001129071.1:p.Arg244=
NM_003238.4:c.646A>C	NP_003229.1:p.Arg216=
NR_138148.1:n.2064A>C
NR_138149.1:n.2148A>C
NM_003238.5:c.646A>C	NP_003229.1:p.Arg216=
NM_003238.6:c.646A>C MANE Select	NP_003229.1:p.Arg216=
NM_001135599.4:c.730A>C	NP_001129071.1:p.Arg244=
NR_138148.2:n.2012A>C
NR_138149.2:n.2096A>C