Canonical Allele Identifier: CA344726726

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218607682A>T (hg19) ; chr1:g.218434340A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.646A>T MANE Select	ENSP00000355897.4:p.Arg216Trp
ENST00000366929.4:c.730A>T	ENSP00000355896.4:p.Arg244Trp
ENST00000366930.8:c.646A>T	ENSP00000355897.4:p.Arg216Trp
ENST00000479322.1:n.130A>T
NM_001135599.2:c.730A>T	NP_001129071.1:p.Arg244Trp
NM_003238.3:c.646A>T	NP_003229.1:p.Arg216Trp
NM_001135599.3:c.730A>T	NP_001129071.1:p.Arg244Trp
NM_003238.4:c.646A>T	NP_003229.1:p.Arg216Trp
NR_138148.1:n.2064A>T
NR_138149.1:n.2148A>T
NM_003238.5:c.646A>T	NP_003229.1:p.Arg216Trp
NM_003238.6:c.646A>T MANE Select	NP_003229.1:p.Arg216Trp
NM_001135599.4:c.730A>T	NP_001129071.1:p.Arg244Trp
NR_138148.2:n.2012A>T
NR_138149.2:n.2096A>T