Canonical Allele Identifier: CA2664866687
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs2125438497
gnomAD v4: 3-30606823-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606823T>G , CM000665.2:g.30606823T>G GRCh38
NC_000003.11:g.30648315T>G , CM000665.1:g.30648315T>G GRCh37
NC_000003.10:g.30623319T>G NCBI36
NG_007490.1:g.5322T>G , LRG_779:g.5322T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-61T>G MANE Select ENSP00000295754.5:n.-61T>G
ENST00000295754.9:c.-61T>G ENSP00000295754.5:n.-61T>G
ENST00000359013.4:c.-61T>G ENSP00000351905.4:n.-61T>G
NM_001024847.2:c.-61T>G , LRG_779t1:c.-61T>G NP_001020018.1:n.-61T>G
NM_003242.5:c.-61T>G NP_003233.4:n.-61T>G
XM_011534045.1:c.-12+230T>G XP_011532347.1:n.-12+230T>G
XM_011534045.3:c.-12+230T>G XP_011532347.1:n.-12+230T>G
NM_003242.6:c.-61T>G MANE Select NP_003233.4:n.-61T>G
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