Canonical Allele Identifier: CA1354851040

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30623239C= , CM000665.2:g.30623239C=	GRCh38
NC_000003.11:g.30664731C= , CM000665.1:g.30664731C=	GRCh37
NC_000003.10:g.30639735C=	NCBI36
NG_007490.1:g.21738C= , LRG_779:g.21738C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.94+16262C= MANE Select	ENSP00000295754.5:n.94+16262C=
ENST00000673250.1:n.184C=
ENST00000295754.9:c.94+16262C=	ENSP00000295754.5:n.94+16262C=
ENST00000359013.4:c.135C=	ENSP00000351905.4:p.Pro45=
NM_001024847.2:c.135C= , LRG_779t1:c.135C=	NP_001020018.1:p.Pro45=
NM_003242.5:c.94+16262C=	NP_003233.4:n.94+16262C=
XM_011534043.1:c.87C=	XP_011532345.1:p.Pro29=
XM_011534044.1:c.46+8533C=	XP_011532346.1:n.46+8533C=
XM_011534045.1:c.-12+16646C=	XP_011532347.1:n.-12+16646C=
XM_011534043.2:c.87C=	XP_011532345.1:p.Pro29=
XM_011534045.3:c.-12+16646C=	XP_011532347.1:n.-12+16646C=
NM_003242.6:c.94+16262C= MANE Select	NP_003233.4:n.94+16262C=