Canonical Allele Identifier: CA1354843279
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606884A= , CM000665.2:g.30606884A= GRCh38
NC_000003.11:g.30648376A= , CM000665.1:g.30648376A= GRCh37
NC_000003.10:g.30623380A= NCBI36
NG_007490.1:g.5383A= , LRG_779:g.5383A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1A= MANE Select ENSP00000295754.5:p.Met1=
ENST00000295754.9:c.1A= ENSP00000295754.5:p.Met1=
ENST00000359013.4:c.1A= ENSP00000351905.4:p.Met1=
NM_001024847.2:c.1A= , LRG_779t1:c.1A= NP_001020018.1:p.Met1=
NM_003242.5:c.1A= NP_003233.4:p.Met1=
XM_011534045.1:c.-12+291A= XP_011532347.1:n.-12+291A=
XM_011534045.3:c.-12+291A= XP_011532347.1:n.-12+291A=
NM_003242.6:c.1A= MANE Select NP_003233.4:p.Met1=