Linked Data
gnomAD v4:
13-53051665-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.53051665C>T , CM000675.2:g.53051665C>T | GRCh38 |
| NC_000013.10:g.53625800C>T , CM000675.1:g.53625800C>T | GRCh37 |
| NC_000013.9:g.52523801C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000219022.3:c.*894C>T MANE Select | ENSP00000219022.2:n.*894C>T | |
| ENST00000219022.2:c.*894C>T | ENSP00000219022.2:n.*894C>T | |
| NM_006418.4:c.*894C>T | NP_006409.3:n.*894C>T | |
| NM_006418.5:c.*894C>T MANE Select | NP_006409.3:n.*894C>T |