Canonical Allele Identifier: CA1354843322
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606964C= , CM000665.2:g.30606964C= GRCh38
NC_000003.11:g.30648456C= , CM000665.1:g.30648456C= GRCh37
NC_000003.10:g.30623460C= NCBI36
NG_007490.1:g.5463C= , LRG_779:g.5463C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.81C= MANE Select ENSP00000295754.5:p.His27=
ENST00000295754.9:c.81C= ENSP00000295754.5:p.His27=
ENST00000359013.4:c.81C= ENSP00000351905.4:p.His27=
NM_001024847.2:c.81C= , LRG_779t1:c.81C= NP_001020018.1:p.His27=
NM_003242.5:c.81C= NP_003233.4:p.His27=
XM_011534045.1:c.-12+371C= XP_011532347.1:n.-12+371C=
XM_011534045.3:c.-12+371C= XP_011532347.1:n.-12+371C=
NM_003242.6:c.81C= MANE Select NP_003233.4:p.His27=