Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.87689686C>T , CM000678.2:g.87689686C>T | GRCh38 |
| NC_000016.9:g.87723292C>T , CM000678.1:g.87723292C>T | GRCh37 |
| NC_000016.8:g.86280793C>T | NCBI36 |
| NG_009797.1:g.91794C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284262.3:c.1326C>T MANE Select | ENSP00000284262.2:p.Asp442= | |
| ENST00000284262.2:c.1326C>T | ENSP00000284262.2:p.Asp442= | |
| ENST00000537256.5:n.1040C>T | ||
| ENST00000563609.1:n.1620C>T | ||
| NM_020655.3:c.1326C>T | NP_065706.2:p.Asp442= | |
| NR_073379.2:n.1040C>T | ||
| XM_006721237.2:c.915C>T | XP_006721300.1:p.Asp305= | |
| NM_020655.4:c.1326C>T MANE Select | NP_065706.2:p.Asp442= | |
| NR_073379.3:n.1040C>T |