Linked Data
gnomAD v4:
12-57450167-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57450167C>T , CM000674.2:g.57450167C>T | GRCh38 |
| NC_000012.11:g.57843950C>T , CM000674.1:g.57843950C>T | GRCh37 |
| NC_000012.10:g.56130217C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309668.3:c.*145C>T MANE Select | ENSP00000308716.2:n.*145C>T | |
| ENST00000309668.2:c.*145C>T | ENSP00000308716.2:n.*145C>T | |
| NM_005538.3:c.*145C>T | NP_005529.1:n.*145C>T | |
| NM_005538.4:c.*145C>T MANE Select | NP_005529.1:n.*145C>T |