Canonical Allele Identifier: CA1354848137

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30616952G= , CM000665.2:g.30616952G=	GRCh38
NC_000003.11:g.30658444G= , CM000665.1:g.30658444G=	GRCh37
NC_000003.10:g.30633448G=	NCBI36
NG_007490.1:g.15451G= , LRG_779:g.15451G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.94+9975G= MANE Select	ENSP00000295754.5:n.94+9975G=
ENST00000673250.1:n.143+2246G=
ENST00000295754.9:c.94+9975G=	ENSP00000295754.5:n.94+9975G=
ENST00000359013.4:c.95-6247G=	ENSP00000351905.4:n.95-6247G=
NM_001024847.2:c.95-6247G= , LRG_779t1:c.95-6247G=	NP_001020018.1:n.95-6247G=
NM_003242.5:c.94+9975G=	NP_003233.4:n.94+9975G=
XM_011534043.1:c.46+2246G=	XP_011532345.1:n.46+2246G=
XM_011534044.1:c.46+2246G=	XP_011532346.1:n.46+2246G=
XM_011534045.1:c.-12+10359G=	XP_011532347.1:n.-12+10359G=
XM_011534043.2:c.46+2246G=	XP_011532345.1:n.46+2246G=
XM_011534045.3:c.-12+10359G=	XP_011532347.1:n.-12+10359G=
NM_003242.6:c.94+9975G= MANE Select	NP_003233.4:n.94+9975G=