Canonical Allele Identifier: CA2147716334
Community Standard Title: NM_003239.5(TGFB3):c.*495C=

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75958692G= , CM000676.2:g.75958692G= GRCh38
NC_000014.8:g.76425035G= , CM000676.1:g.76425035G= GRCh37
NC_000014.7:g.75494788G= NCBI36
NG_011715.1:g.28058C= , LRG_399:g.28058C=

Transcript Alleles

HGVS Amino-acid Change
NM_003239.5:c.*495C= (TGFB3) MANE Select NP_003230.1:n.*495C=
ENST00000238682.8:c.*495C= (TGFB3) MANE Select ENSP00000238682.3:n.*495C=
NM_001329939.1:c.*495C= (TGFB3) NP_001316868.1:n.*495C=
NM_001329939.2:c.*495C= (TGFB3) NP_001316868.1:n.*495C=
NM_003239.3:c.*495C= (TGFB3) NP_003230.1:n.*495C=
NM_003239.4:c.*495C= (TGFB3) NP_003230.1:n.*495C=
ENST00000238682.7:c.*495C= (TGFB3) ENSP00000238682.3:n.*495C=
ENST00000554980.5:n.2115C= (TGFB3)
ENST00000555677.5:n.90-30193G= (IFT43)
ENST00000556674.2:c.*495C= (TGFB3) ENSP00000502685.1:n.*495C=
XM_005268028.1:c.*495C= (TGFB3) XP_005268085.1:n.*495C=