Canonical Allele Identifier: CA1354843148
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606696C= , CM000665.2:g.30606696C= GRCh38
NC_000003.11:g.30648188C= , CM000665.1:g.30648188C= GRCh37
NC_000003.10:g.30623192C= NCBI36
NG_007490.1:g.5195C= , LRG_779:g.5195C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-188C= MANE Select ENSP00000295754.5:n.-188C=
ENST00000295754.9:c.-188C= ENSP00000295754.5:n.-188C=
ENST00000359013.4:c.-188C= ENSP00000351905.4:n.-188C=
NM_001024847.2:c.-188C= , LRG_779t1:c.-188C= NP_001020018.1:n.-188C=
NM_003242.5:c.-188C= NP_003233.4:n.-188C=
XM_011534045.1:c.-12+103C= XP_011532347.1:n.-12+103C=
XM_011534045.3:c.-12+103C= XP_011532347.1:n.-12+103C=
NM_003242.6:c.-188C= MANE Select NP_003233.4:n.-188C=