Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.114683768A>T , CM000674.2:g.114683768A>T | GRCh38 |
| NC_000012.11:g.115121573A>T , CM000674.1:g.115121573A>T | GRCh37 |
| NC_000012.10:g.113605956A>T | NCBI36 |
| NG_008315.1:g.5397T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349155.7:c.-568T>A (TBX3) MANE Select | ENSP00000257567.2:n.-568T>A | |
| ENST00000349155.6:c.-568T>A (TBX3) | ENSP00000257567.2:n.-568T>A | |
| NM_005996.3:c.-568T>A (TBX3) | NP_005987.3:n.-568T>A | |
| NM_016569.3:c.-568T>A (TBX3) | NP_057653.3:n.-568T>A | |
| XR_002957433.1:n.114+1134A>T (TBX3-AS1) | ||
| NM_005996.4:c.-568T>A (TBX3) MANE Select | NP_005987.3:n.-568T>A | |
| NM_016569.4:c.-568T>A (TBX3) | NP_057653.3:n.-568T>A |