Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.99982329G>C , CM000675.2:g.99982329G>C | GRCh38 |
| NC_000013.10:g.100634583G>C , CM000675.1:g.100634583G>C | GRCh37 |
| NC_000013.9:g.99432584G>C | NCBI36 |
| NG_007085.2:g.5265G>C | |
| NG_007085.3:g.5574G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376335.8:c.265G>C MANE Select | ENSP00000365514.3:p.Ala89Pro | |
| ENST00000376335.7:c.265G>C | ENSP00000365514.3:p.Ala89Pro | |
| ENST00000620342.1:c.265G>C | ENSP00000481510.1:p.Ala89Pro | |
| NM_007129.3:c.265G>C | NP_009060.2:p.Ala89Pro | |
| XM_011521110.1:c.265G>C | XP_011519412.1:p.Ala89Pro | |
| NM_007129.4:c.265G>C | NP_009060.2:p.Ala89Pro | |
| NM_007129.5:c.265G>C MANE Select | NP_009060.2:p.Ala89Pro |