Canonical Allele Identifier: CA2147718779

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75961055A= , CM000676.2:g.75961055A= GRCh38
NC_000014.8:g.76427398A= , CM000676.1:g.76427398A= GRCh37
NC_000014.7:g.75497151A= NCBI36
NG_011715.1:g.25695T= , LRG_399:g.25695T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000238682.8:c.948T= (TGFB3) MANE Select ENSP00000238682.3:p.Cys316=
ENST00000556674.2:c.948T= (TGFB3) ENSP00000502685.1:p.Cys316=
ENST00000238682.7:c.948T= (TGFB3) ENSP00000238682.3:p.Cys316=
ENST00000554980.5:n.1329T= (TGFB3)
ENST00000555677.5:n.90-27830A= (IFT43)
ENST00000557493.1:n.414T= (TGFB3)
NM_003239.3:c.948T= (TGFB3) NP_003230.1:p.Cys316=
XM_005268028.1:c.948T= (TGFB3) XP_005268085.1:p.Cys316=
NM_001329939.1:c.948T= (TGFB3) NP_001316868.1:p.Cys316=
NM_003239.4:c.948T= (TGFB3) NP_003230.1:p.Cys316=
NM_001329939.2:c.948T= (TGFB3) NP_001316868.1:p.Cys316=
NM_003239.5:c.948T= (TGFB3) MANE Select NP_003230.1:p.Cys316=