Canonical Allele Identifier: CA2147718369

Gene: TGFB3 IFT43

Linked Data

• dbSNP Id: rs2035144806

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75960651A>C , CM000676.2:g.75960651A>C	GRCh38
NC_000014.8:g.76426994A>C , CM000676.1:g.76426994A>C	GRCh37
NC_000014.7:g.75496747A>C	NCBI36
NG_011715.1:g.26099T>G , LRG_399:g.26099T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000238682.8:c.1080+272T>G (TGFB3) MANE Select	ENSP00000238682.3:n.1080+272T>G
ENST00000556674.2:c.1080+272T>G (TGFB3)	ENSP00000502685.1:n.1080+272T>G
ENST00000238682.7:c.1080+272T>G (TGFB3)	ENSP00000238682.3:n.1080+272T>G
ENST00000554980.5:n.1461+272T>G (TGFB3)
ENST00000555677.5:n.90-28234A>C (IFT43)
ENST00000556507.1:n.36-265T>G (TGFB3)
NM_003239.3:c.1080+272T>G (TGFB3)	NP_003230.1:n.1080+272T>G
XM_005268028.1:c.1080+272T>G (TGFB3)	XP_005268085.1:n.1080+272T>G
NM_001329939.1:c.1080+272T>G (TGFB3)	NP_001316868.1:n.1080+272T>G
NM_003239.4:c.1080+272T>G (TGFB3)	NP_003230.1:n.1080+272T>G
NM_001329939.2:c.1080+272T>G (TGFB3)	NP_001316868.1:n.1080+272T>G
NM_003239.5:c.1080+272T>G (TGFB3) MANE Select	NP_003230.1:n.1080+272T>G