Canonical Allele Identifier: CA1354873147
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672139A= , CM000665.2:g.30672139A= GRCh38
NC_000003.11:g.30713631A= , CM000665.1:g.30713631A= GRCh37
NC_000003.10:g.30688635A= NCBI36
NG_007490.1:g.70638A= , LRG_779:g.70638A=

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.956A= MANE Select ENSP00000295754.5:p.Lys319=
ENST00000672866.1:n.2552A=
ENST00000295754.9:c.956A= ENSP00000295754.5:p.Lys319=
ENST00000359013.4:c.1031A= ENSP00000351905.4:p.Lys344=
NM_001024847.2:c.1031A= , LRG_779t1:c.1031A= NP_001020018.1:p.Lys344=
NM_003242.5:c.956A= NP_003233.4:p.Lys319=
XM_011534043.1:c.983A= XP_011532345.1:p.Lys328=
XM_011534044.1:c.908A= XP_011532346.1:p.Lys303=
XM_011534045.1:c.851A= XP_011532347.1:p.Lys284=
XM_011534043.2:c.983A= XP_011532345.1:p.Lys328=
XM_011534045.3:c.851A= XP_011532347.1:p.Lys284=
XM_017007106.1:c.851A= XP_016862595.1:p.Lys284=
NM_003242.6:c.956A= MANE Select NP_003233.4:p.Lys319=