Canonical Allele Identifier: CA344725094

Gene: TGFB2

Linked Data

• MyVariant Identifiers: chr1:g.218520055T>A (hg19) ; chr1:g.218346713T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346713T>A , CM000663.2:g.218346713T>A	GRCh38
NC_000001.10:g.218520055T>A , CM000663.1:g.218520055T>A	GRCh37
NC_000001.9:g.216586678T>A	NCBI36
NG_027721.1:g.6380T>A
NG_027721.2:g.6380T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.12T>A MANE Select	ENSP00000355897.4:p.Cys4Ter
ENST00000366929.4:c.12T>A	ENSP00000355896.4:p.Cys4Ter
ENST00000366930.8:c.12T>A	ENSP00000355897.4:p.Cys4Ter
NM_001135599.2:c.12T>A	NP_001129071.1:p.Cys4Ter
NM_003238.3:c.12T>A	NP_003229.1:p.Cys4Ter
NM_001135599.3:c.12T>A	NP_001129071.1:p.Cys4Ter
NM_003238.4:c.12T>A	NP_003229.1:p.Cys4Ter
NR_138148.1:n.1430T>A
NR_138149.1:n.1430T>A
NM_003238.5:c.12T>A	NP_003229.1:p.Cys4Ter
NM_003238.6:c.12T>A MANE Select	NP_003229.1:p.Cys4Ter
NM_001135599.4:c.12T>A	NP_001129071.1:p.Cys4Ter
NR_138148.2:n.1378T>A
NR_138149.2:n.1378T>A