Canonical Allele Identifier: CA344725886

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218578528T>G (hg19) ; chr1:g.218405186T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405186T>G , CM000663.2:g.218405186T>G	GRCh38
NC_000001.10:g.218578528T>G , CM000663.1:g.218578528T>G	GRCh37
NC_000001.9:g.216645151T>G	NCBI36
NG_027721.1:g.64853T>G
NG_027721.2:g.64853T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.364T>G MANE Select	ENSP00000355897.4:p.Phe122Val
ENST00000366929.4:c.448T>G	ENSP00000355896.4:p.Phe150Val
ENST00000366930.8:c.364T>G	ENSP00000355897.4:p.Phe122Val
ENST00000488793.1:n.28T>G
NM_001135599.2:c.448T>G	NP_001129071.1:p.Phe150Val
NM_003238.3:c.364T>G	NP_003229.1:p.Phe122Val
NM_001135599.3:c.448T>G	NP_001129071.1:p.Phe150Val
NM_003238.4:c.364T>G	NP_003229.1:p.Phe122Val
NR_138148.1:n.1782T>G
NR_138149.1:n.1866T>G
NM_003238.5:c.364T>G	NP_003229.1:p.Phe122Val
NM_003238.6:c.364T>G MANE Select	NP_003229.1:p.Phe122Val
NM_001135599.4:c.448T>G	NP_001129071.1:p.Phe150Val
NR_138148.2:n.1730T>G
NR_138149.2:n.1814T>G