Canonical Allele Identifier: CA1354873246
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672335T= , CM000665.2:g.30672335T= GRCh38
NC_000003.11:g.30713827T= , CM000665.1:g.30713827T= GRCh37
NC_000003.10:g.30688831T= NCBI36
NG_007490.1:g.70834T= , LRG_779:g.70834T=

Transcript Alleles

HGVS Amino-acid Change
NM_003242.6:c.1152T= MANE Select NP_003233.4:p.Asn384=
ENST00000295754.10:c.1152T= MANE Select ENSP00000295754.5:p.Asn384=
NM_001024847.2:c.1227T= , LRG_779t1:c.1227T= NP_001020018.1:p.Asn409=
NM_003242.5:c.1152T= NP_003233.4:p.Asn384=
ENST00000295754.9:c.1152T= ENSP00000295754.5:p.Asn384=
ENST00000359013.4:c.1227T= ENSP00000351905.4:p.Asn409=
ENST00000672866.1:n.2748T=
XM_011534043.1:c.1179T= XP_011532345.1:p.Asn393=
XM_011534043.2:c.1179T= XP_011532345.1:p.Asn393=
XM_011534044.1:c.1104T= XP_011532346.1:p.Asn368=
XM_011534045.1:c.1047T= XP_011532347.1:p.Asn349=
XM_011534045.3:c.1047T= XP_011532347.1:p.Asn349=
XM_017007106.1:c.1047T= XP_016862595.1:p.Asn349=