Canonical Allele Identifier: CA1354843232
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606810G= , CM000665.2:g.30606810G= GRCh38
NC_000003.11:g.30648302G= , CM000665.1:g.30648302G= GRCh37
NC_000003.10:g.30623306G= NCBI36
NG_007490.1:g.5309G= , LRG_779:g.5309G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-74G= MANE Select ENSP00000295754.5:n.-74G=
ENST00000295754.9:c.-74G= ENSP00000295754.5:n.-74G=
ENST00000359013.4:c.-74G= ENSP00000351905.4:n.-74G=
NM_001024847.2:c.-74G= , LRG_779t1:c.-74G= NP_001020018.1:n.-74G=
NM_003242.5:c.-74G= NP_003233.4:n.-74G=
XM_011534045.1:c.-12+217G= XP_011532347.1:n.-12+217G=
XM_011534045.3:c.-12+217G= XP_011532347.1:n.-12+217G=
NM_003242.6:c.-74G= MANE Select NP_003233.4:n.-74G=