Canonical Allele Identifier: CA351809605

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691478G>C , CM000665.2:g.30691478G>C	GRCh38
NC_000003.11:g.30732970G>C , CM000665.1:g.30732970G>C	GRCh37
NC_000003.10:g.30707974G>C	NCBI36
NG_007490.1:g.89977G>C , LRG_779:g.89977G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.1583G>C MANE Select	NP_003233.4:p.Arg528Pro
ENST00000295754.10:c.1583G>C MANE Select	ENSP00000295754.5:p.Arg528Pro
NM_001024847.2:c.1658G>C , LRG_779t1:c.1658G>C	NP_001020018.1:p.Arg553Pro
NM_003242.5:c.1583G>C	NP_003233.4:p.Arg528Pro
ENST00000295754.9:c.1583G>C	ENSP00000295754.5:p.Arg528Pro
ENST00000359013.4:c.1658G>C	ENSP00000351905.4:p.Arg553Pro
ENST00000672050.1:n.467G>C
ENST00000672866.1:n.3179G>C
ENST00000673203.1:n.461G>C
XM_011534043.1:c.1610G>C	XP_011532345.1:p.Arg537Pro
XM_011534043.2:c.1610G>C	XP_011532345.1:p.Arg537Pro
XM_011534044.1:c.1535G>C	XP_011532346.1:p.Arg512Pro
XM_011534045.1:c.1478G>C	XP_011532347.1:p.Arg493Pro
XM_011534045.3:c.1478G>C	XP_011532347.1:p.Arg493Pro
XM_017007106.1:c.1478G>C	XP_016862595.1:p.Arg493Pro