Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.6780559C= , CM000679.2:g.6780559C= | GRCh38 |
| NC_000017.10:g.6683878C= , CM000679.1:g.6683878C= | GRCh37 |
| NC_000017.9:g.6624602C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_153230.3:c.691C= MANE Select | NP_694962.1:p.Leu231= |
| ENST00000321535.5:c.691C= MANE Select | ENSP00000321386.4:p.Leu231= |
| NM_153230.2:c.691C= | NP_694962.1:p.Leu231= |
| ENST00000321535.4:c.691C= | ENSP00000321386.4:p.Leu231= |
| XM_011523697.1:c.691C= | XP_011521999.1:p.Leu231= |
| XR_243544.3:n.869C= |