Canonical Allele Identifier: CA390467903

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75960987T>G , CM000676.2:g.75960987T>G GRCh38
NC_000014.8:g.76427330T>G , CM000676.1:g.76427330T>G GRCh37
NC_000014.7:g.75497083T>G NCBI36
NG_011715.1:g.25763A>C , LRG_399:g.25763A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000238682.8:c.1016A>C (TGFB3) MANE Select ENSP00000238682.3:p.Tyr339Ser
ENST00000556674.2:c.1016A>C (TGFB3) ENSP00000502685.1:p.Tyr339Ser
ENST00000238682.7:c.1016A>C (TGFB3) ENSP00000238682.3:p.Tyr339Ser
ENST00000554980.5:n.1397A>C (TGFB3)
ENST00000555677.5:n.90-27898T>G (IFT43)
ENST00000557493.1:n.482A>C (TGFB3)
NM_003239.3:c.1016A>C (TGFB3) NP_003230.1:p.Tyr339Ser
XM_005268028.1:c.1016A>C (TGFB3) XP_005268085.1:p.Tyr339Ser
NM_001329939.1:c.1016A>C (TGFB3) NP_001316868.1:p.Tyr339Ser
NM_003239.4:c.1016A>C (TGFB3) NP_003230.1:p.Tyr339Ser
NM_001329939.2:c.1016A>C (TGFB3) NP_001316868.1:p.Tyr339Ser
NM_003239.5:c.1016A>C (TGFB3) MANE Select NP_003230.1:p.Tyr339Ser