Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74259688C= , CM000676.2:g.74259688C= | GRCh38 |
| NC_000014.8:g.74726391C= , CM000676.1:g.74726391C= | GRCh37 |
| NC_000014.7:g.73796144C= | NCBI36 |
| NG_013092.1:g.25217C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261980.3:c.666C= MANE Select | ENSP00000261980.2:p.Tyr222= | |
| ENST00000261980.2:c.666C= | ENSP00000261980.2:p.Tyr222= | |
| NM_182894.2:c.666C= | NP_878314.1:p.Tyr222= | |
| XM_011536719.1:c.666C= | XP_011535021.1:p.Tyr222= | |
| NM_182894.3:c.666C= MANE Select | NP_878314.1:p.Tyr222= |