Canonical Allele Identifier: CA1354851002

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30623148G= , CM000665.2:g.30623148G=	GRCh38
NC_000003.11:g.30664640G= , CM000665.1:g.30664640G=	GRCh37
NC_000003.10:g.30639644G=	NCBI36
NG_007490.1:g.21647G= , LRG_779:g.21647G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.94+16171G= MANE Select	ENSP00000295754.5:n.94+16171G=
ENST00000673250.1:n.144-51G=
ENST00000295754.9:c.94+16171G=	ENSP00000295754.5:n.94+16171G=
ENST00000359013.4:c.95-51G=	ENSP00000351905.4:n.95-51G=
NM_001024847.2:c.95-51G= , LRG_779t1:c.95-51G=	NP_001020018.1:n.95-51G=
NM_003242.5:c.94+16171G=	NP_003233.4:n.94+16171G=
XM_011534043.1:c.47-51G=	XP_011532345.1:n.47-51G=
XM_011534044.1:c.46+8442G=	XP_011532346.1:n.46+8442G=
XM_011534045.1:c.-12+16555G=	XP_011532347.1:n.-12+16555G=
XM_011534043.2:c.47-51G=	XP_011532345.1:n.47-51G=
XM_011534045.3:c.-12+16555G=	XP_011532347.1:n.-12+16555G=
NM_003242.6:c.94+16171G= MANE Select	NP_003233.4:n.94+16171G=