Canonical Allele Identifier: CA1354873244
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672330T= , CM000665.2:g.30672330T= GRCh38
NC_000003.11:g.30713822T= , CM000665.1:g.30713822T= GRCh37
NC_000003.10:g.30688826T= NCBI36
NG_007490.1:g.70829T= , LRG_779:g.70829T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1147T= MANE Select ENSP00000295754.5:p.Ser383=
ENST00000672866.1:n.2743T=
ENST00000295754.9:c.1147T= ENSP00000295754.5:p.Ser383=
ENST00000359013.4:c.1222T= ENSP00000351905.4:p.Ser408=
NM_001024847.2:c.1222T= , LRG_779t1:c.1222T= NP_001020018.1:p.Ser408=
NM_003242.5:c.1147T= NP_003233.4:p.Ser383=
XM_011534043.1:c.1174T= XP_011532345.1:p.Ser392=
XM_011534044.1:c.1099T= XP_011532346.1:p.Ser367=
XM_011534045.1:c.1042T= XP_011532347.1:p.Ser348=
XM_011534043.2:c.1174T= XP_011532345.1:p.Ser392=
XM_011534045.3:c.1042T= XP_011532347.1:p.Ser348=
XM_017007106.1:c.1042T= XP_016862595.1:p.Ser348=
NM_003242.6:c.1147T= MANE Select NP_003233.4:p.Ser383=