Canonical Allele Identifier: CA1354851007
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30623157A= , CM000665.2:g.30623157A= GRCh38
NC_000003.11:g.30664649A= , CM000665.1:g.30664649A= GRCh37
NC_000003.10:g.30639653A= NCBI36
NG_007490.1:g.21656A= , LRG_779:g.21656A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.94+16180A= MANE Select ENSP00000295754.5:n.94+16180A=
ENST00000673250.1:n.144-42A=
ENST00000295754.9:c.94+16180A= ENSP00000295754.5:n.94+16180A=
ENST00000359013.4:c.95-42A= ENSP00000351905.4:n.95-42A=
NM_001024847.2:c.95-42A= , LRG_779t1:c.95-42A= NP_001020018.1:n.95-42A=
NM_003242.5:c.94+16180A= NP_003233.4:n.94+16180A=
XM_011534043.1:c.47-42A= XP_011532345.1:n.47-42A=
XM_011534044.1:c.46+8451A= XP_011532346.1:n.46+8451A=
XM_011534045.1:c.-12+16564A= XP_011532347.1:n.-12+16564A=
XM_011534043.2:c.47-42A= XP_011532345.1:n.47-42A=
XM_011534045.3:c.-12+16564A= XP_011532347.1:n.-12+16564A=
NM_003242.6:c.94+16180A= MANE Select NP_003233.4:n.94+16180A=