Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.82727657C= , CM000679.2:g.82727657C= | GRCh38 |
| NC_000017.10:g.80685533C= , CM000679.1:g.80685533C= | GRCh37 |
| NC_000017.9:g.78278822C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000269373.11:c.*486C= MANE Select | ENSP00000269373.6:n.*486C= | |
| ENST00000269373.10:c.*486C= | ENSP00000269373.6:n.*486C= | |
| ENST00000571594.1:c.53+490C= | ENSP00000459751.1:n.53+490C= | |
| NM_024619.3:c.*486C= | NP_078895.2:n.*486C= | |
| NR_046408.1:n.1594C= | ||
| XM_024450948.1:c.*486C= | XP_024306716.1:n.*486C= | |
| NM_024619.4:c.*486C= MANE Select | NP_078895.2:n.*486C= | |
| NR_046408.2:n.1594C= |