Canonical Allele Identifier: CA2574134790

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441461C>A , CM000663.2:g.218441461C>A	GRCh38
NC_000001.10:g.218614803C>A , CM000663.1:g.218614803C>A	GRCh37
NC_000001.9:g.216681426C>A	NCBI36
NG_027721.1:g.101128C>A
NG_027721.2:g.101128C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.*99C>A MANE Select	ENSP00000355897.4:n.*99C>A
ENST00000366929.4:c.*99C>A	ENSP00000355896.4:n.*99C>A
ENST00000366930.8:c.*99C>A	ENSP00000355897.4:n.*99C>A
ENST00000479322.1:n.828C>A
NM_001135599.2:c.*99C>A	NP_001129071.1:n.*99C>A
NM_003238.3:c.*99C>A	NP_003229.1:n.*99C>A
NM_001135599.3:c.*99C>A	NP_001129071.1:n.*99C>A
NM_003238.4:c.*99C>A	NP_003229.1:n.*99C>A
NR_138148.1:n.2647C>A
NR_138149.1:n.2731C>A
NM_003238.5:c.*99C>A	NP_003229.1:n.*99C>A
NM_003238.6:c.*99C>A MANE Select	NP_003229.1:n.*99C>A
NM_001135599.4:c.*99C>A	NP_001129071.1:n.*99C>A
NR_138148.2:n.2595C>A
NR_138149.2:n.2679C>A