Linked Data
gnomAD v4:
12-52492695-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52492695T>C , CM000674.2:g.52492695T>C | GRCh38 |
| NC_000012.11:g.52886479T>C , CM000674.1:g.52886479T>C | GRCh37 |
| NC_000012.10:g.51172746T>C | NCBI36 |
| NG_008298.1:g.5703A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330722.7:c.494A>G MANE Select | ENSP00000369317.3:p.Glu165Gly | |
| ENST00000330722.6:c.494A>G | ENSP00000369317.3:p.Glu165Gly | |
| ENST00000549898.5:n.15A>G | ||
| NM_005554.3:c.494A>G | NP_005545.1:p.Glu165Gly | |
| NM_005554.4:c.494A>G MANE Select | NP_005545.1:p.Glu165Gly |