Canonical Allele Identifier: CA1354871357
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs3773640

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30668019A>G , CM000665.2:g.30668019A>G GRCh38
NC_000003.11:g.30709511A>G , CM000665.1:g.30709511A>G GRCh37
NC_000003.10:g.30684515A>G NCBI36
NG_007490.1:g.66518A>G , LRG_779:g.66518A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.455-3619A>G MANE Select ENSP00000295754.5:n.455-3619A>G
ENST00000672866.1:n.2051-3619A>G
ENST00000295754.9:c.455-3619A>G ENSP00000295754.5:n.455-3619A>G
ENST00000359013.4:c.530-3619A>G ENSP00000351905.4:n.530-3619A>G
NM_001024847.2:c.530-3619A>G , LRG_779t1:c.530-3619A>G NP_001020018.1:n.530-3619A>G
NM_003242.5:c.455-3619A>G NP_003233.4:n.455-3619A>G
XM_011534043.1:c.482-3619A>G XP_011532345.1:n.482-3619A>G
XM_011534044.1:c.407-3619A>G XP_011532346.1:n.407-3619A>G
XM_011534045.1:c.350-3619A>G XP_011532347.1:n.350-3619A>G
XM_011534043.2:c.482-3619A>G XP_011532345.1:n.482-3619A>G
XM_011534045.3:c.350-3619A>G XP_011532347.1:n.350-3619A>G
XM_017007106.1:c.350-3619A>G XP_016862595.1:n.350-3619A>G
NM_003242.6:c.455-3619A>G MANE Select NP_003233.4:n.455-3619A>G