Canonical Allele Identifier: CA390468185

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75963336C>G , CM000676.2:g.75963336C>G GRCh38
NC_000014.8:g.76429679C>G , CM000676.1:g.76429679C>G GRCh37
NC_000014.7:g.75499432C>G NCBI36
NG_011715.1:g.23414G>C , LRG_399:g.23414G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000238682.8:c.906G>C (TGFB3) MANE Select ENSP00000238682.3:p.Leu302Phe
ENST00000556674.2:c.906G>C (TGFB3) ENSP00000502685.1:p.Leu302Phe
ENST00000238682.7:c.906G>C (TGFB3) ENSP00000238682.3:p.Leu302Phe
ENST00000554980.5:n.1287G>C (TGFB3)
ENST00000555677.5:n.90-25549C>G (IFT43)
ENST00000556285.1:c.906G>C (TGFB3) ENSP00000451110.1:p.Leu302Phe
ENST00000557493.1:n.372G>C (TGFB3)
NM_003239.3:c.906G>C (TGFB3) NP_003230.1:p.Leu302Phe
XM_005268028.1:c.906G>C (TGFB3) XP_005268085.1:p.Leu302Phe
NM_001329938.1:c.906G>C (TGFB3) NP_001316867.1:p.Leu302Phe
NM_001329939.1:c.906G>C (TGFB3) NP_001316868.1:p.Leu302Phe
NM_003239.4:c.906G>C (TGFB3) NP_003230.1:p.Leu302Phe
NM_001329938.2:c.906G>C (TGFB3) NP_001316867.1:p.Leu302Phe
NM_001329939.2:c.906G>C (TGFB3) NP_001316868.1:p.Leu302Phe
NM_003239.5:c.906G>C (TGFB3) MANE Select NP_003230.1:p.Leu302Phe