Canonical Allele Identifier: CA1144233564

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346995_218347009delinsCTACGCCAAGGAGGT , CM000663.2:g.218346995_218347009delinsCTACGCCAAGGAGGT	GRCh38
NC_000001.10:g.218520337_218520351delinsCTACGCCAAGGAGGT , CM000663.1:g.218520337_218520351delinsCTACGCCAAGGAGGT	GRCh37
NC_000001.9:g.216586960_216586974delinsCTACGCCAAGGAGGT	NCBI36
NG_027721.1:g.6662_6676delinsCTACGCCAAGGAGGT
NG_027721.2:g.6662_6676delinsCTACGCCAAGGAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.294_308delinsCTACGCCAAGGAGGT MANE Select	ENSP00000355897.4:p.Tyr98=
ENST00000366929.4:c.294_308delinsCTACGCCAAGGAGGT	ENSP00000355896.4:p.Tyr98=
ENST00000366930.8:c.294_308delinsCTACGCCAAGGAGGT	ENSP00000355897.4:p.Tyr98=
NM_001135599.2:c.294_308delinsCTACGCCAAGGAGGT	NP_001129071.1:p.Tyr98=
NM_003238.3:c.294_308delinsCTACGCCAAGGAGGT	NP_003229.1:p.Tyr98=
NM_001135599.3:c.294_308delinsCTACGCCAAGGAGGT	NP_001129071.1:p.Tyr98=
NM_003238.4:c.294_308delinsCTACGCCAAGGAGGT	NP_003229.1:p.Tyr98=
NR_138148.1:n.1712_1726delinsCTACGCCAAGGAGGT
NR_138149.1:n.1712_1726delinsCTACGCCAAGGAGGT
NM_003238.5:c.294_308delinsCTACGCCAAGGAGGT	NP_003229.1:p.Tyr98=
NM_003238.6:c.294_308delinsCTACGCCAAGGAGGT MANE Select	NP_003229.1:p.Tyr98=
NM_001135599.4:c.294_308delinsCTACGCCAAGGAGGT	NP_001129071.1:p.Tyr98=
NR_138148.2:n.1660_1674delinsCTACGCCAAGGAGGT
NR_138149.2:n.1660_1674delinsCTACGCCAAGGAGGT