Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184056974C>T , CM000665.2:g.184056974C>T | GRCh38 |
| NC_000003.11:g.183774762C>T , CM000665.1:g.183774762C>T | GRCh37 |
| NC_000003.10:g.185257456C>T | NCBI36 |
| NG_012749.1:g.8928C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_130770.3:c.489C>T MANE Select | NP_570126.2:p.Asn163= |
| ENST00000318351.2:c.489C>T MANE Select | ENSP00000322617.1:p.Asn163= |
| NM_130770.2:c.489C>T | NP_570126.2:p.Asn163= |
| ENST00000318351.1:c.489C>T | ENSP00000322617.1:p.Asn163= |