Canonical Allele Identifier: CA1354848194
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30617092A= , CM000665.2:g.30617092A= GRCh38
NC_000003.11:g.30658584A= , CM000665.1:g.30658584A= GRCh37
NC_000003.10:g.30633588A= NCBI36
NG_007490.1:g.15591A= , LRG_779:g.15591A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.94+10115A= MANE Select ENSP00000295754.5:n.94+10115A=
ENST00000673250.1:n.143+2386A=
ENST00000295754.9:c.94+10115A= ENSP00000295754.5:n.94+10115A=
ENST00000359013.4:c.95-6107A= ENSP00000351905.4:n.95-6107A=
NM_001024847.2:c.95-6107A= , LRG_779t1:c.95-6107A= NP_001020018.1:n.95-6107A=
NM_003242.5:c.94+10115A= NP_003233.4:n.94+10115A=
XM_011534043.1:c.46+2386A= XP_011532345.1:n.46+2386A=
XM_011534044.1:c.46+2386A= XP_011532346.1:n.46+2386A=
XM_011534045.1:c.-12+10499A= XP_011532347.1:n.-12+10499A=
XM_011534043.2:c.46+2386A= XP_011532345.1:n.46+2386A=
XM_011534045.3:c.-12+10499A= XP_011532347.1:n.-12+10499A=
NM_003242.6:c.94+10115A= MANE Select NP_003233.4:n.94+10115A=