Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33005847C= , CM000668.2:g.33005847C= | GRCh38 |
| NC_000006.11:g.32973624C= , CM000668.1:g.32973624C= | GRCh37 |
| NC_000006.10:g.33081602C= | NCBI36 |
| NG_012007.1:g.8766G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229829.7:c.*991G= MANE Select | ENSP00000229829.3:n.*991G= | |
| ENST00000229829.6:c.*991G= | ENSP00000229829.3:n.*991G= | |
| NM_002119.3:c.*991G= | NP_002110.1:n.*991G= | |
| NM_002119.4:c.*991G= MANE Select | NP_002110.1:n.*991G= |