Canonical Allele Identifier: CA11356434
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1078985
gnomAD v2: 3-30690911-A-G
gnomAD v3: 3-30649419-A-G
gnomAD v4: 3-30649419-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30649419A>G , CM000665.2:g.30649419A>G GRCh38
NC_000003.11:g.30690911A>G , CM000665.1:g.30690911A>G GRCh37
NC_000003.10:g.30665915A>G NCBI36
NG_007490.1:g.47918A>G , LRG_779:g.47918A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295754.10:c.264-851A>G MANE Select ENSP00000295754.5:n.264-851A>G
ENST00000672866.1:n.1860-851A>G
ENST00000673250.1:n.388-851A>G
ENST00000295754.9:c.264-851A>G ENSP00000295754.5:n.264-851A>G
ENST00000359013.4:c.339-851A>G ENSP00000351905.4:n.339-851A>G
NM_001024847.2:c.339-851A>G , LRG_779t1:c.339-851A>G NP_001020018.1:n.339-851A>G
NM_003242.5:c.264-851A>G NP_003233.4:n.264-851A>G
XM_011534043.1:c.291-851A>G XP_011532345.1:n.291-851A>G
XM_011534044.1:c.216-851A>G XP_011532346.1:n.216-851A>G
XM_011534045.1:c.159-851A>G XP_011532347.1:n.159-851A>G
XM_011534043.2:c.291-851A>G XP_011532345.1:n.291-851A>G
XM_011534045.3:c.159-851A>G XP_011532347.1:n.159-851A>G
XM_017007106.1:c.159-851A>G XP_016862595.1:n.159-851A>G
NM_003242.6:c.264-851A>G MANE Select NP_003233.4:n.264-851A>G