Canonical Allele Identifier: CA7280302

Linked Data

dbSNP Id: rs778996314

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75963289T>A , CM000676.2:g.75963289T>A GRCh38
NC_000014.8:g.76429632T>A , CM000676.1:g.76429632T>A GRCh37
NC_000014.7:g.75499385T>A NCBI36
NG_011715.1:g.23461A>T , LRG_399:g.23461A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000238682.8:c.926+27A>T (TGFB3) MANE Select ENSP00000238682.3:n.926+27A>T
ENST00000556674.2:c.926+27A>T (TGFB3) ENSP00000502685.1:n.926+27A>T
ENST00000238682.7:c.926+27A>T (TGFB3) ENSP00000238682.3:n.926+27A>T
ENST00000554980.5:n.1307+27A>T (TGFB3)
ENST00000555677.5:n.90-25596T>A (IFT43)
ENST00000556285.1:c.*23A>T (TGFB3) ENSP00000451110.1:n.*23A>T
ENST00000557493.1:n.392+27A>T (TGFB3)
NM_003239.3:c.926+27A>T (TGFB3) NP_003230.1:n.926+27A>T
XM_005268028.1:c.926+27A>T (TGFB3) XP_005268085.1:n.926+27A>T
NM_001329938.1:c.*23A>T (TGFB3) NP_001316867.1:n.*23A>T
NM_001329939.1:c.926+27A>T (TGFB3) NP_001316868.1:n.926+27A>T
NM_003239.4:c.926+27A>T (TGFB3) NP_003230.1:n.926+27A>T
NM_001329938.2:c.*23A>T (TGFB3) NP_001316867.1:n.*23A>T
NM_001329939.2:c.926+27A>T (TGFB3) NP_001316868.1:n.926+27A>T
NM_003239.5:c.926+27A>T (TGFB3) MANE Select NP_003230.1:n.926+27A>T