Canonical Allele Identifier: CA1354852758

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30627192A= , CM000665.2:g.30627192A=	GRCh38
NC_000003.11:g.30668684A= , CM000665.1:g.30668684A=	GRCh37
NC_000003.10:g.30643688A=	NCBI36
NG_007490.1:g.25691A= , LRG_779:g.25691A=

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.95-17555A= MANE Select	NP_003233.4:n.95-17555A=
ENST00000295754.10:c.95-17555A= MANE Select	ENSP00000295754.5:n.95-17555A=
NM_001024847.2:c.169+3919A= , LRG_779t1:c.169+3919A=	NP_001020018.1:n.169+3919A=
NM_003242.5:c.95-17555A=	NP_003233.4:n.95-17555A=
ENST00000295754.9:c.95-17555A=	ENSP00000295754.5:n.95-17555A=
ENST00000359013.4:c.169+3919A=	ENSP00000351905.4:n.169+3919A=
ENST00000673250.1:n.218+3919A=
XM_011534043.1:c.121+3919A=	XP_011532345.1:n.121+3919A=
XM_011534043.2:c.121+3919A=	XP_011532345.1:n.121+3919A=
XM_011534044.1:c.46+12486A=	XP_011532346.1:n.46+12486A=
XM_011534045.1:c.-11-17555A=	XP_011532347.1:n.-11-17555A=
XM_011534045.3:c.-11-17555A=	XP_011532347.1:n.-11-17555A=