Canonical Allele Identifier: CA390467623

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75960940C>T , CM000676.2:g.75960940C>T GRCh38
NC_000014.8:g.76427283C>T , CM000676.1:g.76427283C>T GRCh37
NC_000014.7:g.75497036C>T NCBI36
NG_011715.1:g.25810G>A , LRG_399:g.25810G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000238682.8:c.1063G>A (TGFB3) MANE Select ENSP00000238682.3:p.Asp355Asn
ENST00000556674.2:c.1063G>A (TGFB3) ENSP00000502685.1:p.Asp355Asn
ENST00000238682.7:c.1063G>A (TGFB3) ENSP00000238682.3:p.Asp355Asn
ENST00000554980.5:n.1444G>A (TGFB3)
ENST00000555677.5:n.90-27945C>T (IFT43)
ENST00000556507.1:n.18G>A (TGFB3)
ENST00000557493.1:n.529G>A (TGFB3)
NM_003239.3:c.1063G>A (TGFB3) NP_003230.1:p.Asp355Asn
XM_005268028.1:c.1063G>A (TGFB3) XP_005268085.1:p.Asp355Asn
NM_001329939.1:c.1063G>A (TGFB3) NP_001316868.1:p.Asp355Asn
NM_003239.4:c.1063G>A (TGFB3) NP_003230.1:p.Asp355Asn
NM_001329939.2:c.1063G>A (TGFB3) NP_001316868.1:p.Asp355Asn
NM_003239.5:c.1063G>A (TGFB3) MANE Select NP_003230.1:p.Asp355Asn