Canonical Allele Identifier: CA2574134791

Gene: TGFB2

Genomic Alleles

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

Transcript Alleles

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