Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.46837172A= , CM000685.2:g.46837172A= | GRCh38 |
| NC_000023.10:g.46696607A= , CM000685.1:g.46696607A= | GRCh37 |
| NC_000023.9:g.46581551A= | NCBI36 |
| NG_009107.1:g.5261A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218340.4:c.72A= MANE Select | ENSP00000218340.3:p.Pro24= | |
| ENST00000218340.3:c.72A= | ENSP00000218340.3:p.Pro24= | |
| NM_006915.2:c.72A= | NP_008846.2:p.Pro24= | |
| NM_006915.3:c.72A= MANE Select | NP_008846.2:p.Pro24= |