Canonical Allele Identifier: CA351807710
Gene: TGFBR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30671896A>C , CM000665.2:g.30671896A>C GRCh38
NC_000003.11:g.30713388A>C , CM000665.1:g.30713388A>C GRCh37
NC_000003.10:g.30688392A>C NCBI36
NG_007490.1:g.70395A>C , LRG_779:g.70395A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.713A>C MANE Select ENSP00000295754.5:p.Asn238Thr
ENST00000672866.1:n.2309A>C
ENST00000295754.9:c.713A>C ENSP00000295754.5:p.Asn238Thr
ENST00000359013.4:c.788A>C ENSP00000351905.4:p.Asn263Thr
NM_001024847.2:c.788A>C , LRG_779t1:c.788A>C NP_001020018.1:p.Asn263Thr
NM_003242.5:c.713A>C NP_003233.4:p.Asn238Thr
XM_011534043.1:c.740A>C XP_011532345.1:p.Asn247Thr
XM_011534044.1:c.665A>C XP_011532346.1:p.Asn222Thr
XM_011534045.1:c.608A>C XP_011532347.1:p.Asn203Thr
XM_011534043.2:c.740A>C XP_011532345.1:p.Asn247Thr
XM_011534045.3:c.608A>C XP_011532347.1:p.Asn203Thr
XM_017007106.1:c.608A>C XP_016862595.1:p.Asn203Thr
NM_003242.6:c.713A>C MANE Select NP_003233.4:p.Asn238Thr