Canonical Allele Identifier: CA344725887

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218578529T>A (hg19) ; chr1:g.218405187T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218405187T>A , CM000663.2:g.218405187T>A	GRCh38
NC_000001.10:g.218578529T>A , CM000663.1:g.218578529T>A	GRCh37
NC_000001.9:g.216645152T>A	NCBI36
NG_027721.1:g.64854T>A
NG_027721.2:g.64854T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.365T>A MANE Select	ENSP00000355897.4:p.Phe122Tyr
ENST00000366929.4:c.449T>A	ENSP00000355896.4:p.Phe150Tyr
ENST00000366930.8:c.365T>A	ENSP00000355897.4:p.Phe122Tyr
ENST00000488793.1:n.29T>A
NM_001135599.2:c.449T>A	NP_001129071.1:p.Phe150Tyr
NM_003238.3:c.365T>A	NP_003229.1:p.Phe122Tyr
NM_001135599.3:c.449T>A	NP_001129071.1:p.Phe150Tyr
NM_003238.4:c.365T>A	NP_003229.1:p.Phe122Tyr
NR_138148.1:n.1783T>A
NR_138149.1:n.1867T>A
NM_003238.5:c.365T>A	NP_003229.1:p.Phe122Tyr
NM_003238.6:c.365T>A MANE Select	NP_003229.1:p.Phe122Tyr
NM_001135599.4:c.449T>A	NP_001129071.1:p.Phe150Tyr
NR_138148.2:n.1731T>A
NR_138149.2:n.1815T>A