Canonical Allele Identifier: CA351808894

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125438786
• MyVariant Identifiers: chr3:g.30715610G>C (hg19) ; chr3:g.30674118G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674118G>C , CM000665.2:g.30674118G>C	GRCh38
NC_000003.11:g.30715610G>C , CM000665.1:g.30715610G>C	GRCh37
NC_000003.10:g.30690614G>C	NCBI36
NG_007490.1:g.72617G>C , LRG_779:g.72617G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1268G>C MANE Select	ENSP00000295754.5:p.Arg423Thr
ENST00000672866.1:n.2864G>C
ENST00000673203.1:n.146G>C
ENST00000295754.9:c.1268G>C	ENSP00000295754.5:p.Arg423Thr
ENST00000359013.4:c.1343G>C	ENSP00000351905.4:p.Arg448Thr
NM_001024847.2:c.1343G>C , LRG_779t1:c.1343G>C	NP_001020018.1:p.Arg448Thr
NM_003242.5:c.1268G>C	NP_003233.4:p.Arg423Thr
XM_011534043.1:c.1295G>C	XP_011532345.1:p.Arg432Thr
XM_011534044.1:c.1220G>C	XP_011532346.1:p.Arg407Thr
XM_011534045.1:c.1163G>C	XP_011532347.1:p.Arg388Thr
XM_011534043.2:c.1295G>C	XP_011532345.1:p.Arg432Thr
XM_011534045.3:c.1163G>C	XP_011532347.1:p.Arg388Thr
XM_017007106.1:c.1163G>C	XP_016862595.1:p.Arg388Thr
NM_003242.6:c.1268G>C MANE Select	NP_003233.4:p.Arg423Thr