Canonical Allele Identifier: CA433009861
Gene: TGFBR2 HGNC NCBI

Linked Data

dbSNP Id: rs758864131
MyVariant Identifiers: chr3:g.30648381T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606889T>G , CM000665.2:g.30606889T>G GRCh38
NC_000003.11:g.30648381T>G , CM000665.1:g.30648381T>G GRCh37
NC_000003.10:g.30623385T>G NCBI36
NG_007490.1:g.5388T>G , LRG_779:g.5388T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.6T>G MANE Select ENSP00000295754.5:p.Gly2=
ENST00000295754.9:c.6T>G ENSP00000295754.5:p.Gly2=
ENST00000359013.4:c.6T>G ENSP00000351905.4:p.Gly2=
NM_001024847.2:c.6T>G , LRG_779t1:c.6T>G NP_001020018.1:p.Gly2=
NM_003242.5:c.6T>G NP_003233.4:p.Gly2=
XM_011534045.1:c.-12+296T>G XP_011532347.1:n.-12+296T>G
XM_011534045.3:c.-12+296T>G XP_011532347.1:n.-12+296T>G
NM_003242.6:c.6T>G MANE Select NP_003233.4:p.Gly2=