Canonical Allele Identifier: CA351807865
Gene: TGFBR2 HGNC NCBI

Linked Data

COSMIC: COSM78641

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30671969G>C , CM000665.2:g.30671969G>C GRCh38
NC_000003.11:g.30713461G>C , CM000665.1:g.30713461G>C GRCh37
NC_000003.10:g.30688465G>C NCBI36
NG_007490.1:g.70468G>C , LRG_779:g.70468G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.786G>C MANE Select ENSP00000295754.5:p.Lys262Asn
ENST00000672866.1:n.2382G>C
ENST00000295754.9:c.786G>C ENSP00000295754.5:p.Lys262Asn
ENST00000359013.4:c.861G>C ENSP00000351905.4:p.Lys287Asn
NM_001024847.2:c.861G>C , LRG_779t1:c.861G>C NP_001020018.1:p.Lys287Asn
NM_003242.5:c.786G>C NP_003233.4:p.Lys262Asn
XM_011534043.1:c.813G>C XP_011532345.1:p.Lys271Asn
XM_011534044.1:c.738G>C XP_011532346.1:p.Lys246Asn
XM_011534045.1:c.681G>C XP_011532347.1:p.Lys227Asn
XM_011534043.2:c.813G>C XP_011532345.1:p.Lys271Asn
XM_011534045.3:c.681G>C XP_011532347.1:p.Lys227Asn
XM_017007106.1:c.681G>C XP_016862595.1:p.Lys227Asn
NM_003242.6:c.786G>C MANE Select NP_003233.4:p.Lys262Asn