Canonical Allele Identifier: CA1354843185
Gene: TGFBR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30606742C= , CM000665.2:g.30606742C= GRCh38
NC_000003.11:g.30648234C= , CM000665.1:g.30648234C= GRCh37
NC_000003.10:g.30623238C= NCBI36
NG_007490.1:g.5241C= , LRG_779:g.5241C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.-142C= MANE Select ENSP00000295754.5:n.-142C=
ENST00000295754.9:c.-142C= ENSP00000295754.5:n.-142C=
ENST00000359013.4:c.-142C= ENSP00000351905.4:n.-142C=
NM_001024847.2:c.-142C= , LRG_779t1:c.-142C= NP_001020018.1:n.-142C=
NM_003242.5:c.-142C= NP_003233.4:n.-142C=
XM_011534045.1:c.-12+149C= XP_011532347.1:n.-12+149C=
XM_011534045.3:c.-12+149C= XP_011532347.1:n.-12+149C=
NM_003242.6:c.-142C= MANE Select NP_003233.4:n.-142C=
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