Canonical Allele Identifier: CA1354863275

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30649676T= , CM000665.2:g.30649676T=	GRCh38
NC_000003.11:g.30691168T= , CM000665.1:g.30691168T=	GRCh37
NC_000003.10:g.30666172T=	NCBI36
NG_007490.1:g.48175T= , LRG_779:g.48175T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.264-594T= MANE Select	ENSP00000295754.5:n.264-594T=
ENST00000672866.1:n.1860-594T=
ENST00000673250.1:n.388-594T=
ENST00000295754.9:c.264-594T=	ENSP00000295754.5:n.264-594T=
ENST00000359013.4:c.339-594T=	ENSP00000351905.4:n.339-594T=
NM_001024847.2:c.339-594T= , LRG_779t1:c.339-594T=	NP_001020018.1:n.339-594T=
NM_003242.5:c.264-594T=	NP_003233.4:n.264-594T=
XM_011534043.1:c.291-594T=	XP_011532345.1:n.291-594T=
XM_011534044.1:c.216-594T=	XP_011532346.1:n.216-594T=
XM_011534045.1:c.159-594T=	XP_011532347.1:n.159-594T=
XM_011534043.2:c.291-594T=	XP_011532345.1:n.291-594T=
XM_011534045.3:c.159-594T=	XP_011532347.1:n.159-594T=
XM_017007106.1:c.159-594T=	XP_016862595.1:n.159-594T=
NM_003242.6:c.264-594T= MANE Select	NP_003233.4:n.264-594T=