Canonical Allele Identifier: CA1354848146

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30616979T= , CM000665.2:g.30616979T=	GRCh38
NC_000003.11:g.30658471T= , CM000665.1:g.30658471T=	GRCh37
NC_000003.10:g.30633475T=	NCBI36
NG_007490.1:g.15478T= , LRG_779:g.15478T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.94+10002T= MANE Select	ENSP00000295754.5:n.94+10002T=
ENST00000673250.1:n.143+2273T=
ENST00000295754.9:c.94+10002T=	ENSP00000295754.5:n.94+10002T=
ENST00000359013.4:c.95-6220T=	ENSP00000351905.4:n.95-6220T=
NM_001024847.2:c.95-6220T= , LRG_779t1:c.95-6220T=	NP_001020018.1:n.95-6220T=
NM_003242.5:c.94+10002T=	NP_003233.4:n.94+10002T=
XM_011534043.1:c.46+2273T=	XP_011532345.1:n.46+2273T=
XM_011534044.1:c.46+2273T=	XP_011532346.1:n.46+2273T=
XM_011534045.1:c.-12+10386T=	XP_011532347.1:n.-12+10386T=
XM_011534043.2:c.46+2273T=	XP_011532345.1:n.46+2273T=
XM_011534045.3:c.-12+10386T=	XP_011532347.1:n.-12+10386T=
NM_003242.6:c.94+10002T= MANE Select	NP_003233.4:n.94+10002T=