Canonical Allele Identifier: CA2574134611

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218347094_218347097dup , CM000663.2:g.218347094_218347097dup	GRCh38
NC_000001.10:g.218520436_218520439dup , CM000663.1:g.218520436_218520439dup	GRCh37
NC_000001.9:g.216587059_216587062dup	NCBI36
NG_027721.1:g.6761_6764dup
NG_027721.2:g.6761_6764dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.346+47_346+50dup MANE Select	ENSP00000355897.4:n.346+47_346+50dup
ENST00000366929.4:c.346+47_346+50dup	ENSP00000355896.4:n.346+47_346+50dup
ENST00000366930.8:c.346+47_346+50dup	ENSP00000355897.4:n.346+47_346+50dup
ENST00000488793.1:n.10+47_10+50dup
NM_001135599.2:c.346+47_346+50dup	NP_001129071.1:n.346+47_346+50dup
NM_003238.3:c.346+47_346+50dup	NP_003229.1:n.346+47_346+50dup
NM_001135599.3:c.346+47_346+50dup	NP_001129071.1:n.346+47_346+50dup
NM_003238.4:c.346+47_346+50dup	NP_003229.1:n.346+47_346+50dup
NR_138148.1:n.1764+47_1764+50dup
NR_138149.1:n.1764+47_1764+50dup
NM_003238.5:c.346+47_346+50dup	NP_003229.1:n.346+47_346+50dup
NM_003238.6:c.346+47_346+50dup MANE Select	NP_003229.1:n.346+47_346+50dup
NM_001135599.4:c.346+47_346+50dup	NP_001129071.1:n.346+47_346+50dup
NR_138148.2:n.1712+47_1712+50dup
NR_138149.2:n.1712+47_1712+50dup