Canonical Allele Identifier: CA2838000255

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75963492A>T , CM000676.2:g.75963492A>T GRCh38
NC_000014.8:g.76429835A>T , CM000676.1:g.76429835A>T GRCh37
NC_000014.7:g.75499588A>T NCBI36
NG_011715.1:g.23258T>A , LRG_399:g.23258T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000238682.8:c.755-5T>A (TGFB3) MANE Select ENSP00000238682.3:n.755-5T>A
ENST00000556674.2:c.755-5T>A (TGFB3) ENSP00000502685.1:n.755-5T>A
ENST00000238682.7:c.755-5T>A (TGFB3) ENSP00000238682.3:n.755-5T>A
ENST00000554980.5:n.1136-5T>A (TGFB3)
ENST00000555677.5:n.90-25393A>T (IFT43)
ENST00000556285.1:c.755-5T>A (TGFB3) ENSP00000451110.1:n.755-5T>A
ENST00000557493.1:n.221-5T>A (TGFB3)
NM_003239.3:c.755-5T>A (TGFB3) NP_003230.1:n.755-5T>A
XM_005268028.1:c.755-5T>A (TGFB3) XP_005268085.1:n.755-5T>A
NM_001329938.1:c.755-5T>A (TGFB3) NP_001316867.1:n.755-5T>A
NM_001329939.1:c.755-5T>A (TGFB3) NP_001316868.1:n.755-5T>A
NM_003239.4:c.755-5T>A (TGFB3) NP_003230.1:n.755-5T>A
NM_001329938.2:c.755-5T>A (TGFB3) NP_001316867.1:n.755-5T>A
NM_001329939.2:c.755-5T>A (TGFB3) NP_001316868.1:n.755-5T>A
NM_003239.5:c.755-5T>A (TGFB3) MANE Select NP_003230.1:n.755-5T>A