Linked Data
gnomAD v4:
10-133538867-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133538867C>T , CM000672.2:g.133538867C>T | GRCh38 |
| NC_000010.10:g.135352371C>T , CM000672.1:g.135352371C>T | GRCh37 |
| NC_000010.9:g.135202361C>T | NCBI36 |
| NG_008383.1:g.16505C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252945.8:c.1385C>T MANE Select | ENSP00000252945.3:p.Pro462Leu | |
| ENST00000252945.7:c.1385C>T | ENSP00000252945.3:p.Pro462Leu | |
| ENST00000368520.1:n.1358+975C>T | ||
| ENST00000463117.6:c.1385C>T | ENSP00000440689.1:p.Pro462Leu | |
| ENST00000469258.1:n.481C>T | ||
| NM_000773.3:c.1385C>T | NP_000764.1:p.Pro462Leu | |
| NM_000773.4:c.1385C>T MANE Select | NP_000764.1:p.Pro462Leu |