Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52433820G>C , CM000674.2:g.52433820G>C | GRCh38 |
| NC_000012.11:g.52827604G>C , CM000674.1:g.52827604G>C | GRCh37 |
| NC_000012.10:g.51113871G>C | NCBI36 |
| NG_008403.1:g.5507C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252245.6:c.485C>G MANE Select | ENSP00000252245.5:p.Ser162Cys | |
| ENST00000252245.5:c.485C>G | ENSP00000252245.5:p.Ser162Cys | |
| NM_004693.2:c.485C>G | NP_004684.2:p.Ser162Cys | |
| NM_004693.3:c.485C>G MANE Select | NP_004684.2:p.Ser162Cys |