Canonical Allele Identifier: CA2147722662
Community Standard Title: NM_003239.5(TGFB3):c.647-98A=

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75965793T= , CM000676.2:g.75965793T= GRCh38
NC_000014.8:g.76432136T= , CM000676.1:g.76432136T= GRCh37
NC_000014.7:g.75501889T= NCBI36
NG_011715.1:g.20957A= , LRG_399:g.20957A=

Transcript Alleles

HGVS Amino-acid Change
NM_003239.5:c.647-98A= (TGFB3) MANE Select NP_003230.1:n.647-98A=
ENST00000238682.8:c.647-98A= (TGFB3) MANE Select ENSP00000238682.3:n.647-98A=
NM_001329938.1:c.647-98A= (TGFB3) NP_001316867.1:n.647-98A=
NM_001329938.2:c.647-98A= (TGFB3) NP_001316867.1:n.647-98A=
NM_001329939.1:c.647-98A= (TGFB3) NP_001316868.1:n.647-98A=
NM_001329939.2:c.647-98A= (TGFB3) NP_001316868.1:n.647-98A=
NM_003239.3:c.647-98A= (TGFB3) NP_003230.1:n.647-98A=
NM_003239.4:c.647-98A= (TGFB3) NP_003230.1:n.647-98A=
ENST00000238682.7:c.647-98A= (TGFB3) ENSP00000238682.3:n.647-98A=
ENST00000554980.5:n.930A= (TGFB3)
ENST00000555677.5:n.90-23092T= (IFT43)
ENST00000556285.1:c.647-98A= (TGFB3) ENSP00000451110.1:n.647-98A=
ENST00000556674.2:c.647-98A= (TGFB3) ENSP00000502685.1:n.647-98A=
ENST00000557493.1:n.113-98A= (TGFB3)
XM_005268028.1:c.647-98A= (TGFB3) XP_005268085.1:n.647-98A=