Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114713840T= , CM000663.2:g.114713840T= | GRCh38 |
| NC_000001.10:g.115256461T= , CM000663.1:g.115256461T= | GRCh37 |
| NC_000001.9:g.115057984T= | NCBI36 |
| NG_007572.1:g.8055A= , LRG_92:g.8055A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.250A= MANE Select | ENSP00000358548.4:p.Ile84= | |
| ENST00000369535.4:c.250A= | ENSP00000358548.4:p.Ile84= | |
| NM_002524.4:c.250A= | NP_002515.1:p.Ile84= | |
| NM_002524.5:c.250A= MANE Select | NP_002515.1:p.Ile84= |