Canonical Allele Identifier: CA2147718876

Linked Data

dbSNP Id: rs2035152180

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75961139T>C , CM000676.2:g.75961139T>C GRCh38
NC_000014.8:g.76427482T>C , CM000676.1:g.76427482T>C GRCh37
NC_000014.7:g.75497235T>C NCBI36
NG_011715.1:g.25611A>G , LRG_399:g.25611A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000238682.8:c.927-63A>G (TGFB3) MANE Select ENSP00000238682.3:n.927-63A>G
ENST00000556674.2:c.927-63A>G (TGFB3) ENSP00000502685.1:n.927-63A>G
ENST00000238682.7:c.927-63A>G (TGFB3) ENSP00000238682.3:n.927-63A>G
ENST00000554980.5:n.1308-63A>G (TGFB3)
ENST00000555677.5:n.90-27746T>C (IFT43)
ENST00000557493.1:n.393-63A>G (TGFB3)
NM_003239.3:c.927-63A>G (TGFB3) NP_003230.1:n.927-63A>G
XM_005268028.1:c.927-63A>G (TGFB3) XP_005268085.1:n.927-63A>G
NM_001329939.1:c.927-63A>G (TGFB3) NP_001316868.1:n.927-63A>G
NM_003239.4:c.927-63A>G (TGFB3) NP_003230.1:n.927-63A>G
NM_001329939.2:c.927-63A>G (TGFB3) NP_001316868.1:n.927-63A>G
NM_003239.5:c.927-63A>G (TGFB3) MANE Select NP_003230.1:n.927-63A>G