Canonical Allele Identifier: CA2747786987

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218345707_218345709del , CM000663.2:g.218345707_218345709del	GRCh38
NC_000001.10:g.218519049_218519051del , CM000663.1:g.218519049_218519051del	GRCh37
NC_000001.9:g.216585672_216585674del	NCBI36
NG_027721.1:g.5374_5376del
NG_027721.2:g.5374_5376del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-995_-993del MANE Select	ENSP00000355897.4:n.-995_-993del
NM_001135599.2:c.-995_-993del	NP_001129071.1:n.-995_-993del
NM_003238.3:c.-995_-993del	NP_003229.1:n.-995_-993del
NM_001135599.3:c.-995_-993del	NP_001129071.1:n.-995_-993del
NM_003238.4:c.-995_-993del	NP_003229.1:n.-995_-993del
NR_138148.1:n.424_426del
NR_138149.1:n.424_426del
NM_003238.5:c.-995_-993del	NP_003229.1:n.-995_-993del
NM_003238.6:c.-995_-993del MANE Select	NP_003229.1:n.-995_-993del
NM_001135599.4:c.-995_-993del	NP_001129071.1:n.-995_-993del
NR_138148.2:n.372_374del
NR_138149.2:n.372_374del