Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177038A= , CM000678.2:g.177038A= | GRCh38 |
| NC_000016.9:g.227037A= , CM000678.1:g.227037A= | GRCh37 |
| NC_000016.8:g.167037A= | NCBI36 |
| NG_000006.1:g.37901A= | |
| NG_059186.1:g.5388A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.205A= MANE Select | ENSP00000322421.5:p.Asn69= | |
| ENST00000397797.1:c.109A= | ENSP00000380899.1:p.Asn37= | |
| ENST00000472694.1:n.341A= | ||
| ENST00000487791.1:n.174A= | ||
| NM_000558.4:c.205A= | NP_000549.1:p.Asn69= | |
| NM_000558.5:c.205A= MANE Select | NP_000549.1:p.Asn69= |