Canonical Allele Identifier: CA1221528727

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346994_218347009delinsACTACGCCAAGGAGGT , CM000663.2:g.218346994_218347009delinsACTACGCCAAGGAGGT	GRCh38
NC_000001.10:g.218520336_218520351delinsACTACGCCAAGGAGGT , CM000663.1:g.218520336_218520351delinsACTACGCCAAGGAGGT	GRCh37
NC_000001.9:g.216586959_216586974delinsACTACGCCAAGGAGGT	NCBI36
NG_027721.1:g.6661_6676delinsACTACGCCAAGGAGGT
NG_027721.2:g.6661_6676delinsACTACGCCAAGGAGGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000366930.9:c.293_308delinsACTACGCCAAGGAGGT MANE Select	ENSP00000355897.4:p.Tyr98=
ENST00000366929.4:c.293_308delinsACTACGCCAAGGAGGT	ENSP00000355896.4:p.Tyr98=
ENST00000366930.8:c.293_308delinsACTACGCCAAGGAGGT	ENSP00000355897.4:p.Tyr98=
NM_001135599.2:c.293_308delinsACTACGCCAAGGAGGT	NP_001129071.1:p.Tyr98=
NM_003238.3:c.293_308delinsACTACGCCAAGGAGGT	NP_003229.1:p.Tyr98=
NM_001135599.3:c.293_308delinsACTACGCCAAGGAGGT	NP_001129071.1:p.Tyr98=
NM_003238.4:c.293_308delinsACTACGCCAAGGAGGT	NP_003229.1:p.Tyr98=
NR_138148.1:n.1711_1726delinsACTACGCCAAGGAGGT
NR_138149.1:n.1711_1726delinsACTACGCCAAGGAGGT
NM_003238.5:c.293_308delinsACTACGCCAAGGAGGT	NP_003229.1:p.Tyr98=
NM_003238.6:c.293_308delinsACTACGCCAAGGAGGT MANE Select	NP_003229.1:p.Tyr98=
NM_001135599.4:c.293_308delinsACTACGCCAAGGAGGT	NP_001129071.1:p.Tyr98=
NR_138148.2:n.1659_1674delinsACTACGCCAAGGAGGT
NR_138149.2:n.1659_1674delinsACTACGCCAAGGAGGT