Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169542496T>G , CM000663.2:g.169542496T>G | GRCh38 |
| NC_000001.10:g.169511734T>G , CM000663.1:g.169511734T>G | GRCh37 |
| NC_000001.9:g.167778358T>G | NCBI36 |
| NG_011806.1:g.49036A>C , LRG_553:g.49036A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000130.5:c.2594A>C MANE Select | NP_000121.2:p.His865Pro |
| ENST00000367797.9:c.2594A>C MANE Select | ENSP00000356771.3:p.His865Pro |
| NM_000130.4:c.2594A>C , LRG_553t1:c.2594A>C | NP_000121.2:p.His865Pro |
| ENST00000367796.3:c.2609A>C | ENSP00000356770.3:p.His870Pro |
| ENST00000367797.7:c.2594A>C | ENSP00000356771.3:p.His865Pro |
| XM_017000660.2:c.2183A>C | XP_016856149.1:p.His728Pro |