Canonical Allele Identifier: CA049148
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30671694A>G , CM000665.2:g.30671694A>G GRCh38
NC_000003.11:g.30713186A>G , CM000665.1:g.30713186A>G GRCh37
NC_000003.10:g.30688190A>G NCBI36
NG_007490.1:g.70193A>G , LRG_779:g.70193A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.511A>G MANE Select ENSP00000295754.5:p.Ser171Gly
ENST00000672866.1:n.2107A>G
ENST00000295754.9:c.511A>G ENSP00000295754.5:p.Ser171Gly
ENST00000359013.4:c.586A>G ENSP00000351905.4:p.Ser196Gly
NM_001024847.2:c.586A>G , LRG_779t1:c.586A>G NP_001020018.1:p.Ser196Gly
NM_003242.5:c.511A>G NP_003233.4:p.Ser171Gly
XM_011534043.1:c.538A>G XP_011532345.1:p.Ser180Gly
XM_011534044.1:c.463A>G XP_011532346.1:p.Ser155Gly
XM_011534045.1:c.406A>G XP_011532347.1:p.Ser136Gly
XM_011534043.2:c.538A>G XP_011532345.1:p.Ser180Gly
XM_011534045.3:c.406A>G XP_011532347.1:p.Ser136Gly
XM_017007106.1:c.406A>G XP_016862595.1:p.Ser136Gly
NM_003242.6:c.511A>G MANE Select NP_003233.4:p.Ser171Gly