Canonical Allele Identifier: CA2147720262

Gene: TGFB3 IFT43

Linked Data

• dbSNP Id: rs2035174631
• gnomAD v4: 14-75962914-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75962914C>A , CM000676.2:g.75962914C>A	GRCh38
NC_000014.8:g.76429257C>A , CM000676.1:g.76429257C>A	GRCh37
NC_000014.7:g.75499010C>A	NCBI36
NG_011715.1:g.23836G>T , LRG_399:g.23836G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000238682.8:c.926+402G>T (TGFB3) MANE Select	ENSP00000238682.3:n.926+402G>T
ENST00000556674.2:c.926+402G>T (TGFB3)	ENSP00000502685.1:n.926+402G>T
ENST00000238682.7:c.926+402G>T (TGFB3)	ENSP00000238682.3:n.926+402G>T
ENST00000554980.5:n.1307+402G>T (TGFB3)
ENST00000555677.5:n.90-25971C>A (IFT43)
ENST00000557493.1:n.392+402G>T (TGFB3)
NM_003239.3:c.926+402G>T (TGFB3)	NP_003230.1:n.926+402G>T
XM_005268028.1:c.926+402G>T (TGFB3)	XP_005268085.1:n.926+402G>T
NM_001329939.1:c.926+402G>T (TGFB3)	NP_001316868.1:n.926+402G>T
NM_003239.4:c.926+402G>T (TGFB3)	NP_003230.1:n.926+402G>T
NM_001329939.2:c.926+402G>T (TGFB3)	NP_001316868.1:n.926+402G>T
NM_003239.5:c.926+402G>T (TGFB3) MANE Select	NP_003230.1:n.926+402G>T