Canonical Allele Identifier: CA020594

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30672250G>C , CM000665.2:g.30672250G>C	GRCh38
NC_000003.11:g.30713742G>C , CM000665.1:g.30713742G>C	GRCh37
NC_000003.10:g.30688746G>C	NCBI36
NG_007490.1:g.70749G>C , LRG_779:g.70749G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.1067G>C MANE Select	NP_003233.4:p.Arg356Pro
ENST00000295754.10:c.1067G>C MANE Select	ENSP00000295754.5:p.Arg356Pro
NM_001024847.2:c.1142G>C , LRG_779t1:c.1142G>C	NP_001020018.1:p.Arg381Pro
NM_003242.5:c.1067G>C	NP_003233.4:p.Arg356Pro
ENST00000295754.9:c.1067G>C	ENSP00000295754.5:p.Arg356Pro
ENST00000359013.4:c.1142G>C	ENSP00000351905.4:p.Arg381Pro
ENST00000672866.1:n.2663G>C
XM_011534043.1:c.1094G>C	XP_011532345.1:p.Arg365Pro
XM_011534043.2:c.1094G>C	XP_011532345.1:p.Arg365Pro
XM_011534044.1:c.1019G>C	XP_011532346.1:p.Arg340Pro
XM_011534045.1:c.962G>C	XP_011532347.1:p.Arg321Pro
XM_011534045.3:c.962G>C	XP_011532347.1:p.Arg321Pro
XM_017007106.1:c.962G>C	XP_016862595.1:p.Arg321Pro