Canonical Allele Identifier: CA351808342
Gene: TGFBR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672185G>C , CM000665.2:g.30672185G>C GRCh38
NC_000003.11:g.30713677G>C , CM000665.1:g.30713677G>C GRCh37
NC_000003.10:g.30688681G>C NCBI36
NG_007490.1:g.70684G>C , LRG_779:g.70684G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1002G>C MANE Select ENSP00000295754.5:p.Gln334His
ENST00000672866.1:n.2598G>C
ENST00000295754.9:c.1002G>C ENSP00000295754.5:p.Gln334His
ENST00000359013.4:c.1077G>C ENSP00000351905.4:p.Gln359His
NM_001024847.2:c.1077G>C , LRG_779t1:c.1077G>C NP_001020018.1:p.Gln359His
NM_003242.5:c.1002G>C NP_003233.4:p.Gln334His
XM_011534043.1:c.1029G>C XP_011532345.1:p.Gln343His
XM_011534044.1:c.954G>C XP_011532346.1:p.Gln318His
XM_011534045.1:c.897G>C XP_011532347.1:p.Gln299His
XM_011534043.2:c.1029G>C XP_011532345.1:p.Gln343His
XM_011534045.3:c.897G>C XP_011532347.1:p.Gln299His
XM_017007106.1:c.897G>C XP_016862595.1:p.Gln299His
NM_003242.6:c.1002G>C MANE Select NP_003233.4:p.Gln334His