Canonical Allele Identifier: CA432917684

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125438715
• MyVariant Identifiers: chr3:g.30715599G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674107G>C , CM000665.2:g.30674107G>C	GRCh38
NC_000003.11:g.30715599G>C , CM000665.1:g.30715599G>C	GRCh37
NC_000003.10:g.30690603G>C	NCBI36
NG_007490.1:g.72606G>C , LRG_779:g.72606G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1257G>C MANE Select	ENSP00000295754.5:p.Val419=
ENST00000672866.1:n.2853G>C
ENST00000673203.1:n.135G>C
ENST00000295754.9:c.1257G>C	ENSP00000295754.5:p.Val419=
ENST00000359013.4:c.1332G>C	ENSP00000351905.4:p.Val444=
NM_001024847.2:c.1332G>C , LRG_779t1:c.1332G>C	NP_001020018.1:p.Val444=
NM_003242.5:c.1257G>C	NP_003233.4:p.Val419=
XM_011534043.1:c.1284G>C	XP_011532345.1:p.Val428=
XM_011534044.1:c.1209G>C	XP_011532346.1:p.Val403=
XM_011534045.1:c.1152G>C	XP_011532347.1:p.Val384=
XM_011534043.2:c.1284G>C	XP_011532345.1:p.Val428=
XM_011534045.3:c.1152G>C	XP_011532347.1:p.Val384=
XM_017007106.1:c.1152G>C	XP_016862595.1:p.Val384=
NM_003242.6:c.1257G>C MANE Select	NP_003233.4:p.Val419=