Canonical Allele Identifier: CA2147718609

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75960935T= , CM000676.2:g.75960935T= GRCh38
NC_000014.8:g.76427278T= , CM000676.1:g.76427278T= GRCh37
NC_000014.7:g.75497031T= NCBI36
NG_011715.1:g.25815A= , LRG_399:g.25815A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000238682.8:c.1068A= (TGFB3) MANE Select ENSP00000238682.3:p.Thr356=
ENST00000556674.2:c.1068A= (TGFB3) ENSP00000502685.1:p.Thr356=
ENST00000238682.7:c.1068A= (TGFB3) ENSP00000238682.3:p.Thr356=
ENST00000554980.5:n.1449A= (TGFB3)
ENST00000555677.5:n.90-27950T= (IFT43)
ENST00000556507.1:n.23A= (TGFB3)
ENST00000557493.1:n.534A= (TGFB3)
NM_003239.3:c.1068A= (TGFB3) NP_003230.1:p.Thr356=
XM_005268028.1:c.1068A= (TGFB3) XP_005268085.1:p.Thr356=
NM_001329939.1:c.1068A= (TGFB3) NP_001316868.1:p.Thr356=
NM_003239.4:c.1068A= (TGFB3) NP_003230.1:p.Thr356=
NM_001329939.2:c.1068A= (TGFB3) NP_001316868.1:p.Thr356=
NM_003239.5:c.1068A= (TGFB3) MANE Select NP_003230.1:p.Thr356=