Linked Data
gnomAD v4:
12-52488200-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52488200A>T , CM000674.2:g.52488200A>T | GRCh38 |
| NC_000012.11:g.52881984A>T , CM000674.1:g.52881984A>T | GRCh37 |
| NC_000012.10:g.51168251A>T | NCBI36 |
| NG_008298.1:g.10198T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330722.7:c.1425-97T>A MANE Select | ENSP00000369317.3:n.1425-97T>A | |
| ENST00000330722.6:c.1425-97T>A | ENSP00000369317.3:n.1425-97T>A | |
| NM_005554.3:c.1425-97T>A | NP_005545.1:n.1425-97T>A | |
| NM_005554.4:c.1425-97T>A MANE Select | NP_005545.1:n.1425-97T>A |