Canonical Allele Identifier: CA351807801
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1160016010
gnomAD v2: 3-30713431-A-C
gnomAD v3: 3-30671939-A-C
gnomAD v4: 3-30671939-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30671939A>C , CM000665.2:g.30671939A>C GRCh38
NC_000003.11:g.30713431A>C , CM000665.1:g.30713431A>C GRCh37
NC_000003.10:g.30688435A>C NCBI36
NG_007490.1:g.70438A>C , LRG_779:g.70438A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.756A>C MANE Select ENSP00000295754.5:p.Lys252Asn
ENST00000672866.1:n.2352A>C
ENST00000295754.9:c.756A>C ENSP00000295754.5:p.Lys252Asn
ENST00000359013.4:c.831A>C ENSP00000351905.4:p.Lys277Asn
NM_001024847.2:c.831A>C , LRG_779t1:c.831A>C NP_001020018.1:p.Lys277Asn
NM_003242.5:c.756A>C NP_003233.4:p.Lys252Asn
XM_011534043.1:c.783A>C XP_011532345.1:p.Lys261Asn
XM_011534044.1:c.708A>C XP_011532346.1:p.Lys236Asn
XM_011534045.1:c.651A>C XP_011532347.1:p.Lys217Asn
XM_011534043.2:c.783A>C XP_011532345.1:p.Lys261Asn
XM_011534045.3:c.651A>C XP_011532347.1:p.Lys217Asn
XM_017007106.1:c.651A>C XP_016862595.1:p.Lys217Asn
NM_003242.6:c.756A>C MANE Select NP_003233.4:p.Lys252Asn