Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173215G>C , CM000678.2:g.173215G>C | GRCh38 |
| NC_000016.9:g.223214G>C , CM000678.1:g.223214G>C | GRCh37 |
| NC_000016.8:g.163214G>C | NCBI36 |
| NG_000006.1:g.34078G>C | |
| NG_059186.1:g.1565G>C | |
| NG_059271.1:g.5369G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000517.6:c.186G>C MANE Select | NP_000508.1:p.Lys62Asn |
| ENST00000251595.11:c.186G>C MANE Select | ENSP00000251595.6:p.Lys62Asn |
| NM_000517.4:c.186G>C | NP_000508.1:p.Lys62Asn |
| ENST00000251595.10:c.186G>C | ENSP00000251595.6:p.Lys62Asn |
| ENST00000397806.1:c.90G>C | ENSP00000380908.1:p.Lys30Asn |
| ENST00000482565.1:n.322G>C | |
| ENST00000484216.1:n.155G>C |