Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.143316368C>T , CM000669.2:g.143316368C>T | GRCh38 |
| NC_000007.13:g.143013461C>T , CM000669.1:g.143013461C>T | GRCh37 |
| NC_000007.12:g.142723583C>T | NCBI36 |
| NG_009815.1:g.5243C>T | |
| NG_009815.2:g.5243C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650516.2:c.156C>T | ENSP00000498052.2:p.Pro52= | |
| ENST00000343257.7:c.156C>T MANE Select | ENSP00000339867.2:p.Pro52= | |
| ENST00000650516.1:c.156C>T | ENSP00000498052.1:p.Pro52= | |
| ENST00000343257.6:c.156C>T | ENSP00000339867.2:p.Pro52= | |
| NM_000083.2:c.156C>T | NP_000074.2:p.Pro52= | |
| NR_046453.1:n.243C>T | ||
| XM_011515781.1:c.156C>T | XP_011514083.1:p.Pro52= | |
| NM_000083.3:c.156C>T MANE Select | NP_000074.3:p.Pro52= | |
| NR_046453.2:n.258C>T |