Canonical Allele Identifier: CA263703170

Linked Data

dbSNP Id: rs963158813

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75963394A>G , CM000676.2:g.75963394A>G GRCh38
NC_000014.8:g.76429737A>G , CM000676.1:g.76429737A>G GRCh37
NC_000014.7:g.75499490A>G NCBI36
NG_011715.1:g.23356T>C , LRG_399:g.23356T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000238682.8:c.848T>C (TGFB3) MANE Select ENSP00000238682.3:p.Ile283Thr
ENST00000556674.2:c.848T>C (TGFB3) ENSP00000502685.1:p.Ile283Thr
ENST00000238682.7:c.848T>C (TGFB3) ENSP00000238682.3:p.Ile283Thr
ENST00000554980.5:n.1229T>C (TGFB3)
ENST00000555677.5:n.90-25491A>G (IFT43)
ENST00000556285.1:c.848T>C (TGFB3) ENSP00000451110.1:p.Ile283Thr
ENST00000557493.1:n.314T>C (TGFB3)
NM_003239.3:c.848T>C (TGFB3) NP_003230.1:p.Ile283Thr
XM_005268028.1:c.848T>C (TGFB3) XP_005268085.1:p.Ile283Thr
NM_001329938.1:c.848T>C (TGFB3) NP_001316867.1:p.Ile283Thr
NM_001329939.1:c.848T>C (TGFB3) NP_001316868.1:p.Ile283Thr
NM_003239.4:c.848T>C (TGFB3) NP_003230.1:p.Ile283Thr
NM_001329938.2:c.848T>C (TGFB3) NP_001316867.1:p.Ile283Thr
NM_001329939.2:c.848T>C (TGFB3) NP_001316868.1:p.Ile283Thr
NM_003239.5:c.848T>C (TGFB3) MANE Select NP_003230.1:p.Ile283Thr