Canonical Allele Identifier: CA1221568338

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218441168_218441169delinsTC , CM000663.2:g.218441168_218441169delinsTC	GRCh38
NC_000001.10:g.218614510_218614511delinsTC , CM000663.1:g.218614510_218614511delinsTC	GRCh37
NC_000001.9:g.216681133_216681134delinsTC	NCBI36
NG_027721.1:g.100835_100836delinsTC
NG_027721.2:g.100835_100836delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.1087-36_1087-35delinsTC MANE Select	ENSP00000355897.4:n.1087-36_1087-35delinsTC
ENST00000366929.4:c.1171-36_1171-35delinsTC	ENSP00000355896.4:n.1171-36_1171-35delinsTC
ENST00000366930.8:c.1087-36_1087-35delinsTC	ENSP00000355897.4:n.1087-36_1087-35delinsTC
ENST00000479322.1:n.571-36_571-35delinsTC
NM_001135599.2:c.1171-36_1171-35delinsTC	NP_001129071.1:n.1171-36_1171-35delinsTC
NM_003238.3:c.1087-36_1087-35delinsTC	NP_003229.1:n.1087-36_1087-35delinsTC
NM_001135599.3:c.1171-36_1171-35delinsTC	NP_001129071.1:n.1171-36_1171-35delinsTC
NM_003238.4:c.1087-36_1087-35delinsTC	NP_003229.1:n.1087-36_1087-35delinsTC
NR_138148.1:n.2390-36_2390-35delinsTC
NR_138149.1:n.2474-36_2474-35delinsTC
NM_003238.5:c.1087-36_1087-35delinsTC	NP_003229.1:n.1087-36_1087-35delinsTC
NM_003238.6:c.1087-36_1087-35delinsTC MANE Select	NP_003229.1:n.1087-36_1087-35delinsTC
NM_001135599.4:c.1171-36_1171-35delinsTC	NP_001129071.1:n.1171-36_1171-35delinsTC
NR_138148.2:n.2338-36_2338-35delinsTC
NR_138149.2:n.2422-36_2422-35delinsTC