Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.143352054G= , CM000669.2:g.143352054G= | GRCh38 |
| NC_000007.13:g.143049147G= , CM000669.1:g.143049147G= | GRCh37 |
| NC_000007.12:g.142759269G= | NCBI36 |
| NG_009815.1:g.40929G= | |
| NG_009815.2:g.40929G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650516.2:c.*89G= | ENSP00000498052.2:n.*89G= | |
| ENST00000343257.7:c.*89G= MANE Select | ENSP00000339867.2:n.*89G= | |
| ENST00000343257.6:c.*89G= | ENSP00000339867.2:n.*89G= | |
| XM_011515781.1:c.*89G= | XP_011514083.1:n.*89G= | |
| XM_011515782.1:c.*89G= | XP_011514084.1:n.*89G= | |
| NM_000083.3:c.*89G= MANE Select | NP_000074.3:n.*89G= | |
| NR_046453.2:n.3011G= |