Linked Data
gnomAD v4:
12-52487869-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52487869A>T , CM000674.2:g.52487869A>T | GRCh38 |
| NC_000012.11:g.52881653A>T , CM000674.1:g.52881653A>T | GRCh37 |
| NC_000012.10:g.51167920A>T | NCBI36 |
| NG_008298.1:g.10529T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330722.7:c.1546T>A MANE Select | ENSP00000369317.3:p.Ser516Thr | |
| ENST00000330722.6:c.1546T>A | ENSP00000369317.3:p.Ser516Thr | |
| NM_005554.3:c.1546T>A | NP_005545.1:p.Ser516Thr | |
| NM_005554.4:c.1546T>A MANE Select | NP_005545.1:p.Ser516Thr |