Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131877151G>C , CM000668.2:g.131877151G>C | GRCh38 |
| NC_000006.11:g.132198291G>C , CM000668.1:g.132198291G>C | GRCh37 |
| NC_000006.10:g.132239984G>C | NCBI36 |
| NG_008206.1:g.74136G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683687.1:n.755G>C | ||
| ENST00000684536.1:n.381G>C | ||
| ENST00000647893.1:c.1883G>C MANE Select | ENSP00000498074.1:p.Cys628Ser | |
| ENST00000647981.1:n.568G>C | ||
| ENST00000650437.1:c.1374G>C | ||
| ENST00000360971.6:c.1883G>C | ENSP00000354238.2:p.Cys628Ser | |
| ENST00000459624.1:n.927G>C | ||
| ENST00000513998.5:c.*720G>C | ENSP00000422424.1:n.*720G>C | |
| NM_006208.2:c.1883G>C | NP_006199.2:p.Cys628Ser | |
| XM_011535896.1:c.773G>C | XP_011534198.1:p.Cys258Ser | |
| NM_006208.3:c.1883G>C MANE Select | NP_006199.2:p.Cys628Ser |