Canonical Allele Identifier: CA2574134586

Gene: TGFB2

Linked Data

• dbSNP Id: rs2102527189

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346658del , CM000663.2:g.218346658del	GRCh38
NC_000001.10:g.218520000del , CM000663.1:g.218520000del	GRCh37
NC_000001.9:g.216586623del	NCBI36
NG_027721.1:g.6325del
NG_027721.2:g.6325del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-44del MANE Select	ENSP00000355897.4:n.-44del
ENST00000366929.4:c.-44del	ENSP00000355896.4:n.-44del
ENST00000366930.8:c.-44del	ENSP00000355897.4:n.-44del
NM_001135599.2:c.-44del	NP_001129071.1:n.-44del
NM_003238.3:c.-44del	NP_003229.1:n.-44del
NM_001135599.3:c.-44del	NP_001129071.1:n.-44del
NM_003238.4:c.-44del	NP_003229.1:n.-44del
NR_138148.1:n.1375del
NR_138149.1:n.1375del
NM_003238.5:c.-44del	NP_003229.1:n.-44del
NM_003238.6:c.-44del MANE Select	NP_003229.1:n.-44del
NM_001135599.4:c.-44del	NP_001129071.1:n.-44del
NR_138148.2:n.1323del
NR_138149.2:n.1323del