Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.86568232G>T , CM000678.2:g.86568232G>T | GRCh38 |
| NC_000016.9:g.86601838G>T , CM000678.1:g.86601838G>T | GRCh37 |
| NC_000016.8:g.85159339G>T | NCBI36 |
| NG_012025.1:g.5982G>T | |
| NG_012025.2:g.6404G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005251.3:c.897G>T MANE Select | NP_005242.1:p.Pro299= |
| ENST00000649859.1:c.897G>T MANE Select | ENSP00000497759.1:p.Pro299= |
| NM_005251.2:c.897G>T | NP_005242.1:p.Pro299= |
| ENST00000320354.5:c.897G>T | ENSP00000326371.4:p.Pro299= |