Linked Data
gnomAD v4:
12-52487862-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52487862C>T , CM000674.2:g.52487862C>T | GRCh38 |
| NC_000012.11:g.52881646C>T , CM000674.1:g.52881646C>T | GRCh37 |
| NC_000012.10:g.51167913C>T | NCBI36 |
| NG_008298.1:g.10536G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330722.7:c.1553G>A MANE Select | ENSP00000369317.3:p.Gly518Asp | |
| ENST00000330722.6:c.1553G>A | ENSP00000369317.3:p.Gly518Asp | |
| NM_005554.3:c.1553G>A | NP_005545.1:p.Gly518Asp | |
| NM_005554.4:c.1553G>A MANE Select | NP_005545.1:p.Gly518Asp |