Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.70175792T= , CM000679.2:g.70175792T= | GRCh38 |
| NC_000017.10:g.68171933T= , CM000679.1:g.68171933T= | GRCh37 |
| NC_000017.9:g.65683528T= | NCBI36 |
| NG_008798.1:g.11258T= , LRG_328:g.11258T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243457.4:c.753T= MANE Select | ENSP00000243457.2:p.Asn251= | |
| ENST00000243457.3:c.753T= | ENSP00000243457.2:p.Asn251= | |
| ENST00000535240.1:c.753T= | ENSP00000441848.1:p.Asn251= | |
| NM_000891.2:c.753T= , LRG_328t1:c.753T= | NP_000882.1:p.Asn251= | |
| XM_011524779.1:c.753T= | XP_011523081.1:p.Asn251= | |
| NM_000891.3:c.753T= MANE Select | NP_000882.1:p.Asn251= |