Canonical Allele Identifier: CA1354880749

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30689373C= , CM000665.2:g.30689373C=	GRCh38
NC_000003.11:g.30730865C= , CM000665.1:g.30730865C=	GRCh37
NC_000003.10:g.30705869C=	NCBI36
NG_007490.1:g.87872C= , LRG_779:g.87872C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1524+862C= MANE Select	ENSP00000295754.5:n.1524+862C=
ENST00000672050.1:n.408+862C=
ENST00000672866.1:n.3120+862C=
ENST00000673203.1:n.402+862C=
ENST00000295754.9:c.1524+862C=	ENSP00000295754.5:n.1524+862C=
ENST00000359013.4:c.1599+862C=	ENSP00000351905.4:n.1599+862C=
NM_001024847.2:c.1599+862C= , LRG_779t1:c.1599+862C=	NP_001020018.1:n.1599+862C=
NM_003242.5:c.1524+862C=	NP_003233.4:n.1524+862C=
XM_011534043.1:c.1551+862C=	XP_011532345.1:n.1551+862C=
XM_011534044.1:c.1476+862C=	XP_011532346.1:n.1476+862C=
XM_011534045.1:c.1419+862C=	XP_011532347.1:n.1419+862C=
XM_011534043.2:c.1551+862C=	XP_011532345.1:n.1551+862C=
XM_011534045.3:c.1419+862C=	XP_011532347.1:n.1419+862C=
XM_017007106.1:c.1419+862C=	XP_016862595.1:n.1419+862C=
NM_003242.6:c.1524+862C= MANE Select	NP_003233.4:n.1524+862C=