Canonical Allele Identifier: CA647322760
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs2125438636

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30674080G>A , CM000665.2:g.30674080G>A GRCh38
NC_000003.11:g.30715572G>A , CM000665.1:g.30715572G>A GRCh37
NC_000003.10:g.30690576G>A NCBI36
NG_007490.1:g.72579G>A , LRG_779:g.72579G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1255-25G>A MANE Select ENSP00000295754.5:n.1255-25G>A
ENST00000672866.1:n.2851-25G>A
ENST00000673203.1:n.108G>A
ENST00000295754.9:c.1255-25G>A ENSP00000295754.5:n.1255-25G>A
ENST00000359013.4:c.1330-25G>A ENSP00000351905.4:n.1330-25G>A
NM_001024847.2:c.1330-25G>A , LRG_779t1:c.1330-25G>A NP_001020018.1:n.1330-25G>A
NM_003242.5:c.1255-25G>A NP_003233.4:n.1255-25G>A
XM_011534043.1:c.1282-25G>A XP_011532345.1:n.1282-25G>A
XM_011534044.1:c.1207-25G>A XP_011532346.1:n.1207-25G>A
XM_011534045.1:c.1150-25G>A XP_011532347.1:n.1150-25G>A
XM_011534043.2:c.1282-25G>A XP_011532345.1:n.1282-25G>A
XM_011534045.3:c.1150-25G>A XP_011532347.1:n.1150-25G>A
XM_017007106.1:c.1150-25G>A XP_016862595.1:n.1150-25G>A
NM_003242.6:c.1255-25G>A MANE Select NP_003233.4:n.1255-25G>A