Canonical Allele Identifier: CA1046444701

Gene: TGFBR2

Linked Data

• dbSNP Id: rs1698842479

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30649607_30649608del , CM000665.2:g.30649607_30649608del	GRCh38
NC_000003.11:g.30691099_30691100del , CM000665.1:g.30691099_30691100del	GRCh37
NC_000003.10:g.30666103_30666104del	NCBI36
NG_007490.1:g.48106_48107del , LRG_779:g.48106_48107del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.264-663_264-662del MANE Select	ENSP00000295754.5:n.264-663_264-662del
ENST00000672866.1:n.1860-663_1860-662del
ENST00000673250.1:n.388-663_388-662del
ENST00000295754.9:c.264-663_264-662del	ENSP00000295754.5:n.264-663_264-662del
ENST00000359013.4:c.339-663_339-662del	ENSP00000351905.4:n.339-663_339-662del
NM_001024847.2:c.339-663_339-662del , LRG_779t1:c.339-663_339-662del	NP_001020018.1:n.339-663_339-662del
NM_003242.5:c.264-663_264-662del	NP_003233.4:n.264-663_264-662del
XM_011534043.1:c.291-663_291-662del	XP_011532345.1:n.291-663_291-662del
XM_011534044.1:c.216-663_216-662del	XP_011532346.1:n.216-663_216-662del
XM_011534045.1:c.159-663_159-662del	XP_011532347.1:n.159-663_159-662del
XM_011534043.2:c.291-663_291-662del	XP_011532345.1:n.291-663_291-662del
XM_011534045.3:c.159-663_159-662del	XP_011532347.1:n.159-663_159-662del
XM_017007106.1:c.159-663_159-662del	XP_016862595.1:n.159-663_159-662del
NM_003242.6:c.264-663_264-662del MANE Select	NP_003233.4:n.264-663_264-662del