Canonical Allele Identifier: CA1354843169
Gene: TGFBR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606713T= , CM000665.2:g.30606713T= GRCh38
NC_000003.11:g.30648205T= , CM000665.1:g.30648205T= GRCh37
NC_000003.10:g.30623209T= NCBI36
NG_007490.1:g.5212T= , LRG_779:g.5212T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-171T= MANE Select ENSP00000295754.5:n.-171T=
ENST00000295754.9:c.-171T= ENSP00000295754.5:n.-171T=
ENST00000359013.4:c.-171T= ENSP00000351905.4:n.-171T=
NM_001024847.2:c.-171T= , LRG_779t1:c.-171T= NP_001020018.1:n.-171T=
NM_003242.5:c.-171T= NP_003233.4:n.-171T=
XM_011534045.1:c.-12+120T= XP_011532347.1:n.-12+120T=
XM_011534045.3:c.-12+120T= XP_011532347.1:n.-12+120T=
NM_003242.6:c.-171T= MANE Select NP_003233.4:n.-171T=
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