Canonical Allele Identifier: CA351809182

Gene: TGFBR2

Linked Data

• ClinVar Variation Id: 477538
• ClinVar RCV Id: RCV000528001
• dbSNP Id: rs1553631693
• MyVariant Identifiers: chr3:g.30729875G>A (hg19) ; chr3:g.30688383G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30688383G>A , CM000665.2:g.30688383G>A	GRCh38
NC_000003.11:g.30729875G>A , CM000665.1:g.30729875G>A	GRCh37
NC_000003.10:g.30704879G>A	NCBI36
NG_007490.1:g.86882G>A , LRG_779:g.86882G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1397-1G>A MANE Select	ENSP00000295754.5:n.1397-1G>A
ENST00000672050.1:n.281-1G>A
ENST00000672866.1:n.2993-1G>A
ENST00000673203.1:n.275-1G>A
ENST00000295754.9:c.1397-1G>A	ENSP00000295754.5:n.1397-1G>A
ENST00000359013.4:c.1472-1G>A	ENSP00000351905.4:n.1472-1G>A
NM_001024847.2:c.1472-1G>A , LRG_779t1:c.1472-1G>A	NP_001020018.1:n.1472-1G>A
NM_003242.5:c.1397-1G>A	NP_003233.4:n.1397-1G>A
XM_011534043.1:c.1424-1G>A	XP_011532345.1:n.1424-1G>A
XM_011534044.1:c.1349-1G>A	XP_011532346.1:n.1349-1G>A
XM_011534045.1:c.1292-1G>A	XP_011532347.1:n.1292-1G>A
XM_011534043.2:c.1424-1G>A	XP_011532345.1:n.1424-1G>A
XM_011534045.3:c.1292-1G>A	XP_011532347.1:n.1292-1G>A
XM_017007106.1:c.1292-1G>A	XP_016862595.1:n.1292-1G>A
NM_003242.6:c.1397-1G>A MANE Select	NP_003233.4:n.1397-1G>A